Perfume systems

ABSTRACT

The present application relates to perfume raw materials, perfume delivery systems and consumer products comprising such perfume raw materials and/or such perfume delivery systems, as well as processes for making and using such perfume raw materials, perfume delivery systems and consumer products. Such perfume raw materials and compositions, including the delivery systems, disclosed herein expand the perfume communities&#39; options as such perfume raw materials can provide variations on character and such compositions can provide desired odor profiles.

This is a continuation of U.S. patent application Ser. No. 14/484,513, filed Sep. 12, 2014, now U.S. Pat. No. 9,309,487, which is a continuation of U.S. patent application Ser. No. 13/479,341, filed May 24, 2012, now U.S. Pat. No. 8,912,350, which claims the benefit of Provisional U.S. Patent Application 61/500,478, filed Jun. 23, 2011.

FIELD OF INVENTION

The present application relates to perfume raw materials, perfume delivery systems and consumer products comprising such perfume raw materials and/or perfume delivery systems, as well as processes for making and using such perfume raw materials, perfume delivery systems and consumer products.

BACKGROUND OF THE INVENTION

Consumer products may comprise one or more perfumes and/or perfume delivery systems that can mask an undesirable odor and/or provide a desired scent to a product and/or a situs that is contacted with such a product. While current perfumes and perfume delivery systems provide desirable fragrances, consumers continue to seek products that have scents that may be longer lasting and that are tailored to their individual desires (see for example USPA 2007/0275866 A1 and USPA 2008/0305977 A1)—unfortunately the pool of perfume raw materials and perfume delivery systems that is available is still too limited to completely meet the perfume community's needs. Thus, perfumers need an ever larger pool of perfume raw materials and perfume delivery systems.

Applicants believe that the perfume raw materials and perfumes, including the delivery systems, disclosed herein expand the perfume community's options, as such perfume raw materials can provide variations on character and such perfumes can provide desired odor profiles. In certain aspects, such perfume raw materials and/or perfume delivery systems comprising such perfume raw materials may provide variations on character and/or odor profiles that are better than expected as measured by parameters such as headspace analysis (employed to determine perfume delivery system perfume leakage and/or perfume delivery efficiency), C log P, boiling point and/or odor detection threshold.

SUMMARY OF THE INVENTION

The present application relates to perfume raw materials, perfume delivery systems and consumer products comprising such perfume raw materials and/or such perfume delivery systems, as well as processes for making and using such perfume raw materials, perfume delivery systems and consumer products.

DETAILED DESCRIPTION OF THE INVENTION Definitions

As used herein “consumer product” means baby care, beauty care, fabric & home care, family care, feminine care, health care, snack and/or beverage products or devices generally intended to be used or consumed in the form in which it is sold. Such products include but are not limited to diapers, bibs, wipes; products for and/or methods relating to treating hair (human, dog, and/or cat), including, bleaching, coloring, dyeing, conditioning, shampooing, styling; deodorants and antiperspirants; personal cleansing; cosmetics; skin care including application of creams, lotions, and other topically applied products for consumer use including fine fragrances; and shaving products, products for and/or methods relating to treating fabrics, hard surfaces and any other surfaces in the area of fabric and home care, including: air care including air fresheners and scent delivery systems, car care, dishwashing, fabric conditioning (including softening and/or freshening), laundry detergency, laundry and rinse additive and/or care, hard surface cleaning and/or treatment including floor and toilet bowl cleaners, and other cleaning for consumer or institutional use; products and/or methods relating to bath tissue, facial tissue, paper handkerchiefs, and/or paper towels; tampons, feminine napkins; products and/or methods relating to oral care including toothpastes, tooth gels, tooth rinses, denture adhesives, tooth whitening; over-the-counter health care including cough and cold remedies, pain relievers, RX pharmaceuticals, pet health and nutrition; processed food products intended primarily for consumption between customary meals or as a meal accompaniment (non-limiting examples include potato chips, tortilla chips, popcorn, pretzels, corn chips, cereal bars, vegetable chips or crisps, snack mixes, party mixes, multigrain chips, snack crackers, cheese snacks, pork rinds, corn snacks, pellet snacks, extruded snacks and bagel chips); and coffee.

As used herein, the term “cleaning and/or treatment composition” is a subset of consumer products that includes, unless otherwise indicated, beauty care, fabric & home care products. Such products include, but are not limited to, products for treating hair (human, dog, and/or cat), including, bleaching, coloring, dyeing, conditioning, shampooing, styling; deodorants and antiperspirants; personal cleansing; cosmetics; skin care including application of creams, lotions, and other topically applied products for consumer use including fine fragrances; and shaving products, products for treating fabrics, hard surfaces and any other surfaces in the area of fabric and home care, including: air care including air fresheners and scent delivery systems, car care, dishwashing, fabric conditioning (including softening and/or freshening), laundry detergency, laundry and rinse additive and/or care, hard surface cleaning and/or treatment including floor and toilet bowl cleaners, granular or powder-form all-purpose or “heavy-duty” washing agents, especially cleaning detergents; liquid, gel or paste-form all-purpose washing agents, especially the so-called heavy-duty liquid types; liquid fine-fabric detergents; hand dishwashing agents or light duty dishwashing agents, especially those of the high-foaming type; machine dishwashing agents, including the various tablet, granular, liquid and rinse-aid types for household and institutional use; liquid cleaning and disinfecting agents, including antibacterial hand-wash types, cleaning bars, mouthwashes, denture cleaners, dentifrice, car or carpet shampoos, bathroom cleaners including toilet bowl cleaners; hair shampoos and hair-rinses; shower gels, fine fragrances and foam baths and metal cleaners; as well as cleaning auxiliaries such as bleach additives and “stain-stick” or pre-treat types, substrate-laden products such as dryer added sheets, dry and wetted wipes and pads, nonwoven substrates, and sponges; as well as sprays and mists all for consumer or/and institutional use; and/or methods relating to oral care including toothpastes, tooth gels, tooth rinses, denture adhesives, tooth whitening.

As used herein, the term “fabric and/or hard surface cleaning and/or treatment composition” is a subset of cleaning and treatment compositions that includes, unless otherwise indicated, granular or powder-form all-purpose or “heavy-duty” washing agents, especially cleaning detergents; liquid, gel or paste-form all-purpose washing agents, especially the so-called heavy-duty liquid types; liquid fine-fabric detergents; hand dishwashing agents or light duty dishwashing agents, especially those of the high-foaming type; machine dishwashing agents, including the various tablet, granular, liquid and rinse-aid types for household and institutional use; liquid cleaning and disinfecting agents, including antibacterial hand-wash types, cleaning bars, car or carpet shampoos, bathroom cleaners including toilet bowl cleaners; and metal cleaners, fabric conditioning products including softening and/or freshening that may be in liquid, solid and/or dryer sheet form; as well as cleaning auxiliaries such as bleach additives and “stain-stick” or pre-treat types, substrate-laden products such as dryer added sheets, dry and wetted wipes and pads, nonwoven substrates, and sponges; as well as sprays and mists. All of such products which were applicable may be in standard, concentrated or even highly concentrated form even to the extent that such products may in certain aspect be non-aqueous.

As used herein, articles such as “a” and “an” when used in a claim, are understood to mean one or more of what is claimed or described.

As used herein, the terms “include”, “includes” and “including” are meant to be non-limiting.

As used herein, the term “solid” includes granular, powder, bar and tablet product forms.

As used herein, the term “fluid” includes liquid, gel, paste and gas product forms.

As used herein, the term “situs” includes paper products, fabrics, garments, hard surfaces, hair and skin.

Unless otherwise noted, all component or composition levels are in reference to the active portion of that component or composition, and are exclusive of impurities, for example, residual solvents or by-products, which may be present in commercially available sources of such components or compositions.

All percentages and ratios are calculated by weight unless otherwise indicated. All percentages and ratios are calculated based on the total composition unless otherwise indicated. It should be understood that every maximum numerical limitation given throughout this specification includes every lower numerical limitation, as if such lower numerical limitations were expressly written herein. Every minimum numerical limitation given throughout this specification will include every higher numerical limitation, as if such higher numerical limitations were expressly written herein. Every numerical range given throughout this specification will include every narrower numerical range that falls within such broader numerical range, as if such narrower

Perfume Raw Materials (Herein after “PRMs”)

Suitable PRMs include the PRMs listed in Table 1 below and stereoisomers thereof.

TABLE 1 Chemical Structure IUPAC Names Character description 1

(S)-2,2-dimethyl-3-(4-(prop-1-en-2- yl)cyclohex-1-enyl)propanenitrile floral (rose geranium), woody, citrus 2

3-cyclopropyl-2- (cyclopropylmethyl)-2- methylpropanenitrile herbal, minty, vegetable 3

1-(cyclopropylmethyl)cyclo- propanecarbonitrile intense, spicy, minty 4

(S)-3,3-dimethyl-4-(4-(prop-1-en-2- yl)cyclohex-1-enyl)butan-2-one floral, cedarwood 5

3,3-dimethyl-4-((S)-4-(prop-1-en-2- yl)cyclohex-1-enyl)butan-2-(R,S)-ol terpenic, floral (rose, peony) 6

(S)-2,2-dimethyl-3-(4-(prop-1-en-2- yl)cyclohex-1-enyl)propanal floral, ozonic 7

3-cyclopropyl-2-(cyclo- propylmethyl)-2-methylpropanal herbal, minty, fruity 8

3-cyclopropyl-2-(cyclopro- pylmethyl)-2-methylpropan-1-ol spicy, eugenol 9

(S)-2,2-dimethyl-3-(4-(prop-1-en-2- yl)cyclohex-1-enyl)propan-1-ol floral (whitefloral), terpenic 10

(R,S)-2,2-di(cyclohex-2- enyl)propanenitrile mint (menthone), floral (geranium) 11

(R,S)-2,2-di(cyclohex-2- enyl)acetonitrile minty, herbal 12

1-cyclopropyl-2-(cyclopropylme- thyl)-2,4-(R,S)-dimethylhexan-3-one green, vegetable, medicinal, intense 13

1-(1-(cyclopropyl- methyl)cyclopropyl)ethanone minty, fresh, intense 14

1-(1-(cyclopropylmethyl)- cyclopropyl)pentan-1-one spicy (celery) 15

2-methyl-2-((1R,S)(5R)-2-methyl-5- (prop-1-en-2-yl)cyclohex-2- enyl)propanenitrile fresh, green (agrestic), herbal (chamomile) 16

1-(1-(cyclopropylmethyl)- cyclopropyl)pentan-1-(R,S)ol green, earthy 17

2-methyl-2-((1,R,S)(5R)-2-methyl-5- (prop-1-en-2-yl)cyclohex-2- enyl)propanal fresh, herbal, sulfury, truffle 18

3-((1R,5S)-6,6- dimethylbicyclo[3.1.1]hept-2-en-2- yl)propanenitrile woody, pine, intense 19

(2R,S)-3-((1R,5S)-6,6- dimethylbicyclo[3.1.1]hept-2-en-2- yl)-2-methylpropanenitrile woody, ionone 20

1-(((1R,5S)-6,6-dimethyl- bicyclo[3.1.1]hept-2-en-2-yl)- methyl)cyclobutanecarbonitrile pine, terpenic 21

2-methyl-2-((1,R,S)(5R)-2-methyl-5- (prop-1-en-2-yl)cyclohex-2- enyl)propan-1-ol floral (lily), minty 22

2-allyl-2-methylpent-4-enenitrile herbal, geranium, minty, green 23

4-allyl-4-methylnon-1-en-5-one fruity, green, herbal 24

4-allyl-4-methylnon-1-en-5-(R,S)-ol floral, herbal, baby lotion 25

iso-butyl 2,5-dimethylhex-4-enoate floral, fruity 26

7-cyclopentylideneheptan-2-one green, metallic 27

8-cyclopentylideneoctan-3-one green, vegetable 28

(E/Z)-11-methyldodec-8-en-3-one (9:1-E:Z) floral, fruity, waxy 29

(E/Z)-10-methylundec-7-en-2-one (9:1-E:Z) fruity, herbal, parsley 30

(E/Z)-10-methylundec-7-en-2-(R,S)- ol (9:1-E:Z) green, aromatic, herbal, plastic 31

propyl 7-methyloct-6-enoate fruity, floral, clean linen 32

methyl 7-methyloct-6-enoate fruity, fresh, clean, cucumber green 33

ethyl 7-methyloct-6-enoate fruity (citrus, pineapple), fresh 34

1,5,5-trimethyl-3(R,S)-(3-methylbut- 2-enyloxy)cyclohex-1-ene green, herbal, terpenic 35

(E,Z)-3-((1R,5S)-6,6- dimethylbicyclo[3.1.1]hept-2-en-2- yl)acrylonitrile woody, spicy, iris 36

(E,Z)(R,S)-5-(4-methylcyclohex-3- enyl)hex-2-enenitrile citrus, green, fresh, intense 37

methyl 9-methyldec-6-enoate waxy, fruity, herbal 38

4-((1R,5S)-6,6- dimethylbicyclo[3.1.1]hept-2-en-2- yl)butanenitrile leathery, cedar wood 39

3-((1R,5S)-6,6- dimethylbicyclo[3.1.1]hept-2-en-2- yl)propanal mussel, oyster, ozonic 40

4-((1R,5S)-6,6- dimethylbicyclo[3.1.1]hept-2-en-2- yl)butanal aldehydic, floral, physalis 41

4-((1R,5S)-6,6- dimethylbicyclo[3.1.1]hept-2-en-2- yl)-2-methylbutanenitrile terpenic, pine, clean 42

4-((1R,5S)-6,6- dimethylbicyclo[3.1.1]hept-2-en-2- yl)-2-methylbutanal woody, floral 43

((1R,2R,4R,6S)-7,7- dimethyltricyclo[4.1.1.0^(2,4)]octan-2- yl)methanol woody, terpenic 44

(1R,2R,4R,6S)-2-(methoxymethyl)- 7,7 dimethyl tricyclo[4.1.1.0^(2,4)]octane wood dust, sulphuric 45

1-(3-methylbut-2-en-1- yl)cyclopropanecarbaldehyde minty, herbal 46

2-(1-(3-methylbut-2-en-1- yl)cyclopropyl)-1,3-dioxane herbal (chamomile), aromatic, cigar 47

2-(1-(3-methylbut-2-en-1- yl)cyclopropyl)-1,3-dioxolane aromatic, herbal, fennel 48

2,2,6-trimethylhept-5-enenitrile herbal, vegetable, sharp 49

3,3,7-trimethyloct-6-en-2-one citrus, fruity, clean 50

1-(4-methylpent-3-en-1- yl)cyclobutanecarbonitrile spicy, vegetable, mushroom 51

3,3,7-trimethyloct-6-en-2-(R,S)-ol citrus, lilac, clean 52

1-(1-(4-methylpent-3-en-1- yl)cyclobutyl)ethanone fruity (cassis), woody 53

1-(4-methylpent-3-en-1- yl)cyclobutanecarbaldehyde green, hay, floral 54

1-(R,S)-(1-(4-methylpent-3-en-1- yl)cyclobutyl)ethanol solventy (glue), floral (jasmin) 55

7-(R,S)-methoxy-2,6,6-trimethyloct- 2-ene herbal, mango skin 56

1-(4-methylpent-3-en-1- yl)cyclopropanecarbonitrile minty, spicy, coumarin 57

1-(1-(4-methylpent-3-en-1- yl)cyclopropyl)ethanone grapefruit, wood 58

1-(1-(4-methylpent-3-en-1- yl)cyclopropyl)pentan-l-one Green, ivy leaves 59

1-(R,S)-(1-(4-methylpent-3-en-1- yl)cyclopropyl)ethanol floral rose (peony) 60

8-methylnon-7-en-2-one clean linen, fruity 61

2,6-dimethyl-2-(4-methylpent-3-en- 1-yl)hept-5-enenitrile floral (geranium, violet) 62

6-methylhept-5-enenitrile citrus, spice nitrile 63

2-(R,S),6-dimethylhept-5-enenitrile herbal, minty 64

2,6-dimethyl-2-(4-methylpent-3-en- 1-yl)hept-5-enal ozonic (mussel), fresh 65

2-(R,S),6-dimethyl-2-(3-methylbut-2- en-1-yl)hept-5-enenitrile floral, herbal, clean 66

2-(R,S)-allyl-2,5-dimethylhex-4- enenitrile floral (violet), cucumber, lavender 67

3-(R,S)-allyl-3,6-dimethylhept-5-en- 2-one herbal (lavender), aromatic 68

3-allyl-3,6-dimethylhept-5-en-2-ol humus, earthy 69

2-(R,S)-allyl-2,5-dimethylhex-4-enal floral, tea, liquorice 70

3-ethoxy-4-hydroxybenzonitrile sweet, vanilla-like 71

1-(3-ethoxy-4- hydroxyphenyl)ethanone vanillin, phenolic 72

2-ethoxy-4-(1-(R,S)- hydroxyethyl)phenol vanillin, phenolic 73

(E)-1-(2,4,4-trimethyl-7- oxabicyclo[4.1.0]heptan-3-yl)but-2- en-1-one diffusive 74

(E)-1-(5-hydroxy-4-methoxy-2,2,6- trimethylcyclohexyl)but-2-en-1-one fruity, rum, jam 75

2-ethoxy-4-(4-(R,S)-methyl-1,3- (R,S)-dioxan-2-yl)phenol sweet, woody, phenolic 76

4-(5,5-dimethyl-1,3-dioxan-2-yl)-2- ethoxyphenol sweet, chemical, vanilla 77

4-(4,4-dimethyl-1,3-(R,S)-dioxan-2- yl)-2-ethoxyphenol Sweet, phenolic, balsamic 78

2-ethoxy-4-(4-(R,S)-ethyl-1,3-(R,S)- dioxolan-2-yl)phenol sweet, phenolic, spicy 79

2-ethoxy-4-(4-(R,S)-methyl-1,3- (R,S)-dioxolan-2-yl)phenol sweet, balsamic 80

4-(4,5-(R,S)-dimethyl-1,3-dioxolan- 2-yl)-2-ethoxyphenol sweet, balsamic 81

4-(4-(R,S)-(tert-butyl)-1,3-(R,S)- dioxolan-2-yl)-2-ethoxyphenol woody, spicy, sweet 82

4-(1,3-dioxolan-2-yl)-2- ethoxyphenol sweet, woody, smoked ham 83

4-(1,3-dioxan-2-yl)-2-ethoxyphenol woody (guaiac), sweet, spicy 84

3-butoxy-4-hydroxybenzaldehyde spicy, sweet 85

2-ethoxy-4-(1,3-(R,S)-oxathiolan-2- yl)phenol sulphuric, grapefruit, mercaptan like 86

4-(4-(R,S)-butyl-1,3-(R,S)-dioxolan- 2-yl)-2-ethoxyphenol floral (chrysant), sweet 87

4-hydroxy-3- (pentyloxy)benzaldehyde horsy, sweet, spicy 88

3-ethoxy-4-methoxybenzaldehyde sweet (vanilla-tonka), balsamic 89

3-ethoxy-4-methoxybenzonitrile sweet, costus 90

2-(3-ethoxy-4-methoxyphenyl)-4- methyl-1,3-(R,S)-dioxolane sweet, spicy 91

2-(3-ethoxy-4-methoxyphenyl)-4,5- (R,S)-dimethyl-1,3-dioxolane sweet 92

(E)-1-(5-hydroxy-2,2,6- trimethylcyclohex-3-en-1-yl)but-2- en-1-one fruity, floral 93

2-(R,S)-isopropyl-2,5-dimethylhex-4- enenitrile woody, herbal, intense 94

2-(R,S)-isopropyl-2,6-dimethylhept- 5-enenitrile floral, ozonic (metallic)

The PRMs disclosed in Table 1 above (a.k.a., molecules—as referred to in the Examples section) may provide one or more of the following benefits at levels that Applicants believe are unexpected in view of PRMs in general: neat product odor; wet fabric odor when applied to a fabric; dry fabric odor when applied to a fabric; reduced leakage from an encapsulate, including an encapsulate such as a perfume microcapsule; increased head space versus neat oil in certain perfume delivery technologies; odor when used in a matrix perfume delivery that is applied to a package; neat product odor when applied to a cleaning and/or treatment composition; fine fragrance composition odor when used in a fine fragrance; dry hair odor when a composition comprising such a PRM is applied to hair; PRM bloom from a solution comprising such a PRM; and new PRM character when applied to a situs. Confirmation of such benefits can be obtained by applying standard test methodologies detailed herein. The PRMs and stereoisomers of such PRMs disclosed in Table 1 above can be made in accordance with the teachings detailed in the present specification.

In one aspect, PRMs disclosed herein may have the structure of Table 1 Nos. 1-94. More specifically, PRMs disclosed herein may have the structure of Table 1 Nos. 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 12, 13, 14, 15, 16, 18, 19, 20, 23, 24, 25, 26, 27, 28, 29, 30, 31, 34, 36, 41, 42, 44, 46, 47, 50, 51, 52, 53, 54, 55, 56, 57, 58, 59, 61, 64, 65, 66, 67, 68, 69, 71, 72, 73, 74, 77, 78, 81, 85, 86, 90, 91, 93, 94, and stereoisomers thereof.

In another aspect, the PRMs disclosed in Table 1 and stereoisomers thereof are suitable for use, as defined by the present specification, in consumer products at levels, based on total consumer product weight, of from about 0.0001% to about 25%, from about 0.0005% to about 10%, from about 0.001% to about 5%, from about 0.005% to about 2.5%, or even from 0.01% to about 1%. Such PRMs and stereoisomers thereof may be used in various combinations in the aforementioned consumer products. In one aspect, a consumer product may comprise one or more PRMs selected from Table 1 Nos. 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 40, 41, 42, 43, 44, 45, 46, 47, 48, 49, 60, 62, 63, 64, 65, 66, 67, 68, 69, 71, 72, 73, 74, 75, 77, 78, 81, 82, 83, 85, 86, 87, 89, 90, 91, 92, 93, 94 and stereoisomers thereof.

In another aspect, the PRMs disclosed in Table 1 and stereoisomers thereof are suitable for use, as defined by the present specification, in cleaning and/or treatment compositions at levels, based on total cleaning and treatment products weight of from about 0.0001% to about 25%, from about 0.0005% to about 10%, from about 0.001% to about 5%, from about 0.005% to about 2.5%, or even from 0.01% to about 1%. Such PRMs and stereoisomers thereof may be used in various combinations in the aforementioned cleaning and/treatment compositions. In one aspect, a cleaning and/or treatment composition may comprise one or more PRMs selected from Table 1 Nos. 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 40, 41, 42, 43, 44, 45, 46, 47, 48, 49, 60, 62, 63, 64, 65, 66, 67, 68, 69, 70, 71, 72, 73, 74, 75, 76, 77, 78, 79, 80, 81, 82, 83, 84, 85, 86, 87, 88, 89, 90, 91, 92, 93, 94 and stereoisomers thereof.

In another aspect, the PRMs disclosed in Table 1 and stereoisomers thereof are suitable for use, as defined by the present specification, in fabric and/or hard surface cleaning and/or treatment compositions at levels, based on total fabric and/or hard surface cleaning and/or treatment composition weight of from about 0.00001% to about 25%, from 0.00005% to about 10%, from 0.0001% to about 5%, from 0.0005% to about 1.0%, or even from 0.001% to about 0.5%. Such PRMs and stereoisomers thereof may be used in various combinations in the aforementioned fabric and/or hard surface cleaning and/or treatment compositions. In one aspect, a fabric and/or hard surface cleaning and/or treatment composition may comprise one or more PRMs selected from Table 1 Nos. 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39, 40, 41, 42, 43, 44, 45, 46, 47, 48, 49, 60, 62, 63, 64, 65, 66, 67, 68, 69, 70, 71, 72, 73, 74, 75, 76, 77, 78, 79, 80, 81, 82, 83, 84, 85, 86, 87, 88, 89, 90, 91, 92, 93, 94 and stereoisomers thereof.

In another aspect, a detergent that may comprise the same level of the PRMs as disclosed for the aforementioned fabric and hard surface cleaning and/or treatment compositions is disclosed. In one aspect, a detergent may comprise one or more PRMs selected from Table 1 Nos. 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 40, 41, 42, 43, 44, 45, 46, 47, 48, 49, 60, 62, 63, 64, 65, 66, 67, 68, 69, 70, 71, 72, 73, 74, 75, 76, 77, 78, 79, 80, 81, 82, 83, 84, 85, 86, 87, 88, 89, 90, 91, 92, 93, 94 and stereoisomers thereof.

In another aspect, the PRMs disclosed in Table 1 and stereoisomers thereof are suitable for use in highly compacted consumer products, including highly compacted fabric and hard surface cleaning and/or treatment compositions. For example, the PRMs disclosed in Table 1 and stereoisomers thereof may be employed in solid or fluid highly compacted detergents at levels of from about 0.00001% to about 25%, from 0.00005% to about 10%, from 0.0001% to about 5%, from 0.0005% to about 1.0%, or even from 0.001% to about 0.5%, based on total composition weight. Such PRMs and stereoisomers thereof may be used in various combinations in the aforementioned highly compacted detergent compositions. Such highly compact detergents typically comprise a higher than normal percentage of active ingredients. In one aspect, a highly compacted detergent may comprise one or more PRMs selected from Table 1 Nos. 1-94 and stereoisomers thereof. More specifically, a highly compacted detergent may comprise one or more PRMs selected from Table 1 Nos. 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 40, 41, 42, 43, 44, 45, 46, 47, 48, 49, 60, 62, 63, 64, 65, 66, 67, 68, 69, 70, 71, 72, 73, 74, 75, 76, 77, 78, 79, 80, 81, 82, 83, 84, 85, 86, 87, 88, 89, 90, 91, 92, 93, 94 and stereoisomers thereof.

Perfume Delivery Systems

Certain perfume delivery systems, methods of making certain perfume delivery systems and the uses of such perfume delivery systems are disclosed in USPA 2007/0275866 A1. Such perfume delivery systems include:

I. Polymer Assisted Delivery (PAD): This perfume delivery technology uses polymeric materials to deliver perfume materials. Classical coacervation, water soluble or partly soluble to insoluble charged or neutral polymers, liquid crystals, hot melts, hydrogels, perfumed plastics, microcapsules, nano- and micro-latexes, polymeric film formers, and polymeric absorbents, polymeric adsorbents, etc. are some examples. PAD includes but is not limited to:

-   -   a.) Matrix Systems: The fragrance is dissolved or dispersed in a         polymer matrix or particle. Perfumes, for example, may be 1)         dispersed into the polymer prior to formulating into the product         or 2) added separately from the polymer during or after         formulation of the product. Diffusion of perfume from the         polymer is a common trigger that allows or increases the rate of         perfume release from a polymeric matrix system that is deposited         or applied to the desired surface (situs), although many other         triggers are know that may control perfume release. Absorption         and/or adsorption into or onto polymeric particles, films,         solutions, and the like are aspects of this technology. Nano- or         micro-particles composed of organic materials (e.g., latexes)         are examples. Suitable particles include a wide range of         materials including, but not limited to polyacetal,         polyacrylate, polyacrylic, polyacrylonitrile, polyamide,         polyaryletherketone, polybutadiene, polybutylene, polybutylene         terephthalate, polychloroprene, poly ethylene, polyethylene         terephthalate, polycyclohexylene dimethylene terephthalate,         polycarbonate, polychloroprene, polyhydroxyalkanoate,         polyketone, polyester, polyethylene, polyetherimide,         polyethersulfone, polyethylenechlorinates, polyimide,         polyisoprene, polylactic acid, polymethylpentene, polyphenylene         oxide, polyphenylene sulfide, polyphthalamide, polypropylene,         polystyrene, polysulfone, polyvinyl acetate, polyvinyl chloride,         as well as polymers or copolymers based on         acrylonitrile-butadiene, cellulose acetate, ethylene-vinyl         acetate, ethylene vinyl alcohol, styrene-butadiene, vinyl         acetate-ethylene, and mixtures thereof.

“Standard” systems refer to those that are “pre-loaded” with the intent of keeping the pre-loaded perfume associated with the polymer until the moment or moments of perfume release. Such polymers may also suppress the neat product odor and provide a bloom and/or longevity benefit depending on the rate of perfume release. One challenge with such systems is to achieve the ideal balance between 1) in-product stability (keeping perfume inside carrier until you need it) and 2) timely release (during use or from dry situs). Achieving such stability is particularly important during in-product storage and product aging. This challenge is particularly apparent for aqueous-based, surfactant-containing products, such as heavy duty liquid laundry detergents. Many “Standard” matrix systems available effectively become “Equilibrium” systems when formulated into aqueous-based products. One may select an “Equilibrium” system or a Reservoir system, which has acceptable in-product diffusion stability and available triggers for release (e.g., friction). “Equilibrium” systems are those in which the perfume and polymer may be added separately to the product, and the equilibrium interaction between perfume and polymer leads to a benefit at one or more consumer touch points (versus a free perfume control that has no polymer-assisted delivery technology). The polymer may also be pre-loaded with perfume; however, part or all of the perfume may diffuse during in-product storage reaching an equilibrium that includes having desired perfume raw materials (PRMs) associated with the polymer. The polymer then carries the perfume to the surface, and release is typically via perfume diffusion. The use of such equilibrium system polymers has the potential to decrease the neat product odor intensity of the neat product (usually more so in the case of pre-loaded standard system). Deposition of such polymers may serve to “flatten” the release profile and provide increased longevity. As indicated above, such longevity would be achieved by suppressing the initial intensity and may enable the formulator to use more high impact or low odor detection threshold (ODT) or low Kovats Index (KI) PRMs to achieve FMOT benefits without initial intensity that is too strong or distorted. It is important that perfume release occurs within the time frame of the application to impact the desired consumer touch point or touch points. Suitable micro-particles and micro-latexes as well as methods of making same may be found in USPA 2005/0003980 A1. Matrix systems also include hot melt adhesives and perfume plastics. In addition, hydrophobically modified polysaccharides may be formulated into the perfumed product to increase perfume deposition and/or modify perfume release. All such matrix systems, including for example polysaccarides and nanolatexes may be combined with other PDTs, including other PAD systems such as PAD reservoir systems in the form of a perfume microcapsule (PMC). Polymer Assisted Delivery (PAD) matrix systems may include those described in the following references: US Patent Applications 2004/0110648 A1; 2004/0092414 A1; 2004/0091445 A1 and 2004/0087476 A1; and U.S. Pat. Nos. 6,531,444; 6,024,943; 6,042,792; 6,051,540; 4,540,721 and 4,973,422.

Silicones are also examples of polymers that may be used as PDT, and can provide perfume benefits in a manner similar to the polymer-assisted delivery “matrix system”. Such a PDT is referred to as silicone-assisted delivery (SAD). One may pre-load silicones with perfume, or use them as an equilibrium system as described for PAD. Suitable silicones as well as making same may be found in WO 2005/102261; USPA 20050124530A1; USPA 20050143282A1; and WO 2003/015736. Functionalized silicones may also be used as described in USPA 2006/003913 A1. Examples of silicones include polydimethylsiloxane and polyalkyldimethylsiloxanes. Other examples include those with amine functionality, which may be used to provide benefits associated with amine-assisted delivery (AAD) and/or polymer-assisted delivery (PAD) and/or amine-reaction products (ARP). Other such examples may be found in U.S. Pat. No. 4,911,852; USPA 2004/0058845 A1; USPA 2004/0092425 A1 and USPA 2005/0003980 A1.

-   -   b.) Reservoir Systems: Reservoir systems are also known as a         core-shell type technology, or one in which the fragrance is         surrounded by a perfume release controlling membrane, which may         serve as a protective shell. The material inside the         microcapsule is referred to as the core, internal phase, or         fill, whereas the wall is sometimes called a shell, coating, or         membrane. Microparticles or pressure sensitive capsules or         microcapsules are examples of this technology. Microcapsules of         the current invention are formed by a variety of procedures that         include, but are not limited to, coating, extrusion,         spray-drying, interfacial, in-situ and matrix polymerization.         The possible shell materials vary widely in their stability         toward water. Among the most stable are polyoxymethyleneurea         (PMU)-based materials, which may hold certain PRMs for even long         periods of time in aqueous solution (or product). Such systems         include but are not limited to urea-formaldehyde and/or         melamine-formaldehyde. Stable shell materials include         polyacrylate-based materials obtained as reaction product of an         oil soluble or dispersible amine with a multifunctional acrylate         or methacrylate monomer or oligomer, an oil soluble acid and an         initiator, in presence of an anionic emulsifier comprising a         water soluble or water dispersible acrylic acid alkyl acid         copolymer, an alkali or alkali salt. Gelatin-based microcapsules         may be prepared so that they dissolve quickly or slowly in         water, depending for example on the degree of cross-linking.         Many other capsule wall materials are available and vary in the         degree of perfume diffusion stability observed. Without wishing         to be bound by theory, the rate of release of perfume from a         capsule, for example, once deposited on a surface is typically         in reverse order of in-product perfume diffusion stability. As         such, urea-formaldehyde and melamine-formaldehyde microcapsules         for example, typically require a release mechanism other than,         or in addition to, diffusion for release, such as mechanical         force (e.g., friction, pressure, shear stress) that serves to         break the capsule and increase the rate of perfume (fragrance)         release. Other triggers include melting, dissolution, hydrolysis         or other chemical reaction, electromagnetic radiation, and the         like. The use of pre-loaded microcapsules requires the proper         ratio of in-product stability and in-use and/or on-surface         (on-situs) release, as well as proper selection of PRMs.         Microcapsules that are based on urea-formaldehyde and/or         melamine-formaldehyde are relatively stable, especially in near         neutral aqueous-based solutions. These materials may require a         friction trigger which may not be applicable to all product         applications. Other microcapsule materials (e.g., gelatin) may         be unstable in aqueous-based products and may even provide         reduced benefit (versus free perfume control) when in-product         aged. Scratch and sniff technologies are yet another example of         PAD. Perfume microcapsules (PMC) may include those described in         the following references: US Patent Applications: 2003/0125222         A1; 2003/215417 A1; 2003/216488 A1; 2003/158344 A1; 2003/165692         A1; 2004/071742 A1; 2004/071746 A1; 2004/072719 A1; 2004/072720         A1; 2006/0039934 A1; 2003/203829 A1; 2003/195133 A1; 2004/087477         A1; 2004/0106536 A1; and U.S. Pat. Nos. 6,645,479 B1; 6,200,949         B1; 4,882,220; 4,917,920; 4,514,461; 6,106,875 and 4,234,627,         3,594,328 and US RE 32713, PCT Patent Application: WO         2009/134234 A1, WO 2006/127454 A2, WO 2010/079466 A2, WO         2010/079467 A2, WO 2010/079468 A2, WO 2010/084480 A2.         II. Molecule-Assisted Delivery (MAD): Non-polymer materials or         molecules may also serve to improve the delivery of perfume.         Without wishing to be bound by theory, perfume may         non-covalently interact with organic materials, resulting in         altered deposition and/or release. Non-limiting examples of such         organic materials include but are not limited to hydrophobic         materials such as organic oils, waxes, mineral oils, petrolatum,         fatty acids or esters, sugars, surfactants, liposomes and even         other perfume raw material (perfume oils), as well as natural         oils, including body and/or other soils. Perfume fixatives are         yet another example. In one aspect, non-polymeric materials or         molecules have a C Log P greater than about 2. Molecule-Assisted         Delivery (MAD) may also include those described in U.S. Pat. No.         7,119,060 and U.S. Pat. No. 5,506,201.         III. Fiber-Assisted Delivery (FAD): The choice or use of a situs         itself may serve to improve the delivery of perfume. In fact,         the situs itself may be a perfume delivery technology. For         example, different fabric types such as cotton or polyester will         have different properties with respect to ability to attract         and/or retain and/or release perfume. The amount of perfume         deposited on or in fibers may be altered by the choice of fiber,         and also by the history or treatment of the fiber, as well as by         any fiber coatings or treatments. Fibers may be woven and         non-woven as well as natural or synthetic. Natural fibers         include those produced by plants, animals, and geological         processes, and include but are not limited to cellulose         materials such as cotton, linen, hemp jute, flax, ramie, and         sisal, and fibers used to manufacture paper and cloth.         Fiber-Assisted Delivery may consist of the use of wood fiber,         such as thermomechanical pulp and bleached or unbleached kraft         or sulfite pulps. Animal fibers consist largely of particular         proteins, such as silk, sinew, catgut and hair (including wool).         Polymer fibers based on synthetic chemicals include but are not         limited to polyamide nylon, PET or PBT polyester,         phenol-formaldehyde (PF), polyvinyl alcohol fiber (PVOH),         polyvinyl chloride fiber (PVC), polyolefins (PP and PE), and         acrylic polymers. All such fibers may be pre-loaded with a         perfume, and then added to a product that may or may not contain         free perfume and/or one or more perfume delivery technologies.         In one aspect, the fibers may be added to a product prior to         being loaded with a perfume, and then loaded with a perfume by         adding a perfume that may diffuse into the fiber, to the         product. Without wishing to be bound by theory, the perfume may         absorb onto or be adsorbed into the fiber, for example, during         product storage, and then be released at one or more moments of         truth or consumer touch points.         IV. Amine Assisted Delivery (AAD): The amine-assisted delivery         technology approach utilizes materials that contain an amine         group to increase perfume deposition or modify perfume release         during product use. There is no requirement in this approach to         pre-complex or pre-react the perfume raw material(s) and amine         prior to addition to the product. In one aspect,         amine-containing AAD materials suitable for use herein may be         non-aromatic; for example, polyalkylimine, such as         polyethyleneimine (PEI), or polyvinylamine (PVAm), or aromatic,         for example, anthranilates. Such materials may also be polymeric         or non-polymeric. In one aspect, such materials contain at least         one primary amine. This technology will allow increased         longevity and controlled release also of low ODT perfume notes         (e.g., aldehydes, ketones, enones) via amine functionality, and         delivery of other PRMs, without being bound by theory, via         polymer-assisted delivery for polymeric amines. Without         technology, volatile top notes can be lost too quickly, leaving         a higher ratio of middle and base notes to top notes. The use of         a polymeric amine allows higher levels of top notes and other         PRMS to be used to obtain freshness longevity without causing         neat product odor to be more intense than desired, or allows top         notes and other PRMs to be used more efficiently. In one aspect,         AAD systems are effective at delivering PRMs at pH greater than         about neutral. Without wishing to be bound by theory, conditions         in which more of the amines of the AAD system are deprotonated         may result in an increased affinity of the deprotonated amines         for PRMs such as aldehydes and ketones, including unsaturated         ketones and enones such as damascone. In another aspect,         polymeric amines are effective at delivering PRMs at pH less         than about neutral. Without wishing to be bound by theory,         conditions in which more of the amines of the AAD system are         protonated may result in a decreased affinity of the protonated         amines for PRMs such as aldehydes and ketones, and a strong         affinity of the polymer framework for a broad range of PRMs. In         such an aspect, polymer-assisted delivery may be delivering more         of the perfume benefit; such systems are a subspecies of AAD and         may be referred to as Amine-Polymer-Assisted Delivery or APAD.         In some cases when the APAD is employed in a composition that         has a pH of less than seven, such APAD systems may also be         considered Polymer-Assisted Delivery (PAD). In yet another         aspect, AAD and PAD systems may interact with other materials,         such as anionic surfactants or polymers to form coacervate         and/or coacervates-like systems. In another aspect, a material         that contains a heteroatom other than nitrogen, for example         sulfur, phosphorus or selenium, may be used as an alternative to         amine compounds. In yet another aspect, the aforementioned         alternative compounds can be used in combination with amine         compounds. In yet another aspect, a single molecule may comprise         an amine moiety and one or more of the alternative heteroatom         moieties, for example, thiols, phosphines and selenols. Suitable         AAD systems as well as methods of making same may be found in US         Patent Applications 2005/0003980 A1; 2003/0199422 A1;         2003/0036489 A1; 2004/0220074 A1 and U.S. Pat. No. 6,103,678.         V. Cyclodextrin Delivery System (CD): This technology approach         uses a cyclic oligosaccharide or cyclodextrin to improve the         delivery of perfume. Typically a perfume and cyclodextrin (CD)         complex is formed. Such complexes may be preformed, formed         in-situ, or formed on or in the situs. Without wishing to be         bound by theory, loss of water may serve to shift the         equilibrium toward the CD-Perfume complex, especially if other         adjunct ingredients (e.g., surfactant) are not present at high         concentration to compete with the perfume for the cyclodextrin         cavity. A bloom benefit may be achieved if water exposure or an         increase in moisture content occurs at a later time point. In         addition, cyclodextrin allows the perfume formulator increased         flexibility in selection of PRMs. Cyclodextrin may be pre-loaded         with perfume or added separately from perfume to obtain the         desired perfume stability, deposition or release benefit.         Suitable CDs as well as methods of making same may be found in         USPA 2005/0003980 A1 and 2006/0263313 A1 and U.S. Pat. Nos.         5,552,378; 3,812,011; 4,317,881; 4,418,144 and 4,378,923.         VI. Starch Encapsulated Accord (SEA): The use of a starch         encapsulated accord (SEA) technology allows one to modify the         properties of the perfume, for example, by converting a liquid         perfume into a solid by adding ingredients such as starch. The         benefit includes increased perfume retention during product         storage, especially under non-aqueous conditions. Upon exposure         to moisture, a perfume bloom may be triggered. Benefits at other         moments of truth may also be achieved because the starch allows         the product formulator to select PRMs or PRM concentrations that         normally cannot be used without the presence of SEA. Another         technology example includes the use of other organic and         inorganic materials, such as silica to convert perfume from         liquid to solid. Suitable SEAs as well as methods of making same         may be found in USPA 2005/0003980 A1 and U.S. Pat. No. 6,458,754         B1.         VII. Inorganic Carrier Delivery System (ZIC): This technology         relates to the use of porous zeolites or other inorganic         materials to deliver perfumes. Perfume-loaded zeolite may be         used with or without adjunct ingredients used for example to         coat the perfume-loaded zeolite (PLZ) to change its perfume         release properties during product storage or during use or from         the dry situs. Suitable zeolite and inorganic carriers as well         as methods of making same may be found in USPA 2005/0003980 A1         and U.S. Pat. Nos. 5,858,959; 6,245,732 B1; 6,048,830 and         4,539,135. Silica is another form of ZIC. Another example of a         suitable inorganic carrier includes inorganic tubules, where the         perfume or other active material is contained within the lumen         of the nano- or micro-tubules. In one aspect, the perfume-loaded         inorganic tubule (or Perfume-Loaded Tubule or PLT) is a mineral         nano- or micro-tubule, such as halloysite or mixtures of         halloysite with other inorganic materials, including other         clays. The PLT technology may also comprise additional         ingredients on the inside and/or outside of the tubule for the         purpose of improving in-product diffusion stability, deposition         on the desired situs or for controlling the release rate of the         loaded perfume. Monomeric and/or polymeric materials, including         starch encapsulation, may be used to coat, plug, cap, or         otherwise encapsulate the PLT. Suitable PLT systems as well as         methods of making same may be found in U.S. Pat. No. 5,651,976.         VIII. Pro-Perfume (PP): This technology refers to perfume         technologies that result from the reaction of perfume materials         with other substrates or chemicals to form materials that have a         covalent bond between one or more PRMs and one or more carriers.         The PRM is converted into a new material called a pro-PRM (i.e.,         pro-perfume), which then may release the original PRM upon         exposure to a trigger such as water or light. Pro-perfumes may         provide enhanced perfume delivery properties such as increased         perfume deposition, longevity, stability, retention, and the         like. Pro-perfumes include those that are monomeric         (non-polymeric) or polymeric, and may be pre-formed or may be         formed in-situ under equilibrium conditions, such as those that         may be present during in-product storage or on the wet or dry         situs. Nonlimiting examples of pro-perfumes include Michael         adducts (e.g., beta-amino ketones), aromatic or non-aromatic         imines (Schiff bases), oxazolidines, beta-keto esters, and         orthoesters. Another aspect includes compounds comprising one or         more beta-oxy or beta-thio carbonyl moieties capable of         releasing a PRM, for example, an alpha, beta-unsaturated ketone,         aldehyde or carboxylic ester. The typical trigger for perfume         release is exposure to water; although other triggers may         include enzymes, heat, light, pH change, autoxidation, a shift         of equilibrium, change in concentration or ionic strength and         others. For aqueous-based products, light-triggered pro-perfumes         are particularly suited. Such photo-pro-perfumes (PPPs) include         but are not limited to those that release coumarin derivatives         and perfumes and/or pro-perfumes upon being triggered. The         released pro-perfume may release one or more PRMs by means of         any of the above mentioned triggers. In one aspect, the         photo-pro-perfume releases a nitrogen-based pro-perfume when         exposed to a light and/or moisture trigger. In another aspect,         the nitrogen-based pro-perfume, released from the         photo-pro-perfume, releases one or more PRMs selected, for         example, from aldehydes, ketones (including enones) and         alcohols. In still another aspect, the PPP releases a dihydroxy         coumarin derivative. The light-triggered pro-perfume may also be         an ester that releases a coumarin derivative and a perfume         alcohol. In one aspect the pro-perfume is a dimethoxybenzoin         derivative as described in USPA 2006/0020459 A1. In another         aspect the pro-perfume is a 3′, 5′-dimethoxybenzoin (DMB)         derivative that releases an alcohol upon exposure to         electromagnetic radiation. In yet another aspect, the         pro-perfume releases one or more low ODT PRMs, including         tertiary alcohols such as linalool, tetrahydrolinalool, or         dihydromyrcenol. Suitable pro-perfumes and methods of making         same can be found in U.S. Pat. Nos. 7,018,978 B2; 6,987,084 B2;         6,956,013 B2; 6,861,402 B1; 6,544,945 B1; 6,093,691; 6,277,796         B1; 6,165,953; 6,316,397 B1; 6,437,150 B1; 6,479,682 B1;         6,096,918; 6,218,355 B1; 6,133,228; 6,147,037; 7,109,153 B2;         7,071,151 B2; 6,987,084 B2; 6,610,646 B2 and 5,958,870, as well         as can be found in USPA 2005/0003980 A1 and USPA 2006/0223726         A1.         a.) Amine Reaction Product (ARP): For purposes of the present         application, ARP is a subclass or species of PP. One may also         use “reactive” polymeric amines in which the amine functionality         is pre-reacted with one or more PRMs to form an amine reaction         product (ARP). Typically the reactive amines are primary and/or         secondary amines, and may be part of a polymer or a monomer         (non-polymer). Such ARPs may also be mixed with additional PRMs         to provide benefits of polymer-assisted delivery and/or         amine-assisted delivery. Nonlimiting examples of polymeric         amines include polymers based on polyalkylimines, such as         polyethyleneimine (PEI), or polyvinylamine (PVAm). Nonlimiting         examples of monomeric (non-polymeric) amines include hydroxyl         amines, such as 2-aminoethanol and its alkyl substituted         derivatives, and aromatic amines such as anthranilates. The ARPs         may be premixed with perfume or added separately in leave-on or         rinse-off applications. In another aspect, a material that         contains a heteroatom other than nitrogen, for example oxygen,         sulfur, phosphorus or selenium, may be used as an alternative to         amine compounds. In yet another aspect, the aforementioned         alternative compounds can be used in combination with amine         compounds. In yet another aspect, a single molecule may comprise         an amine moiety and one or more of the alternative heteroatom         moieties, for example, thiols, phosphines and selenols. The         benefit may include improved delivery of perfume as well as         controlled perfume release. Suitable ARPs as well as methods of         making same can be found in USPA 2005/0003980 A1 and U.S. Pat.         No. 6,413,920 B1.

In one aspect, the PRMs disclosed in Table 1 and stereoisomers thereof are suitable for use in perfume delivery systems at levels, based on total perfume delivery system weight, of from 0.001% to about 50%, from 0.005% to 30%, from 0.01% to about 10%, from 0.025% to about 5%, or even from 0.025% to about 1%.

In another aspect, the perfume delivery systems disclosed herein are suitable for use in consumer products, cleaning and treatment compositions, fabric and hard surface cleaning and/or treatment compositions, detergents, and highly compacted consumer products, including highly compacted fabric and hard surface cleaning and/or treatment compositions (e.g., solid or fluid highly compacted detergents) at levels, based on total consumer product weight, from about 0.001% to about 20%, from about 0.01% to about 10%, from about 0.05% to about 5%, from about 0.1% to about 0.5%.

In another aspect, the amount of PRMs from Table 1 present in the perfume delivery systems, based on the total microcapsule and/or nanocapsule (Polymer Assisted Delivery (PAD) Reservoir System) weight, may be from about 0.1% to about 99%, from 25% to about 95%, from 30 to about 90%, from 45% to about 90%, or from 65% to about 90%. In one aspect, microcapsules and/or nanocapsules may comprise one or more PRMs selected from Table 1 Nos. 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39, 40, 41, 42, 43, 44, 45, 46, 47, 48, 49, 60, 62, 63, 64, 65, 66, 67, 68, 69, 71, 72; stereoisomers of Table 1 Nos. 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39, 40, 41, 42, 43, 44, 45, 46, 47, 48, 49, 60, 62, 63, 64, 65, 66, 67, 68, 69, 70, 71, 72, 73, 74, 75, 76, 77, 78, 79, 80, 81, 82, 83, 84, 85, 86, 87, 88, 89, 90, 91, 92, 93, 94; and mixtures thereof.

PRM Nos. 4, 12, 13, 14, 23, 26, 27, 28, 29, 49, 52, 57, 58, 60, 67, 71, 73, 74 and 92 are ketones. PRM Nos. 6, 7, 17, 39, 40, 42, 45, 53, 64, 69, 84, 87 and 88 are aldehydes. PRM Nos. 5, 8, 9, 16, 21, 24, 30, 43, 51, 54, 59, 68, 72, 75, 76, 77, 78, 79, 80, 81, 82, 83, 85, and 86 are alcohols. PRM Nos. 25, 31, 32, 33, 37, 44 and 55 are esters. PRM Nos. 1, 2, 3, 10, 11, 15, 18, 19, 20, 22, 35, 36, 38, 41, 48, 50, 56, 61, 62, 63, 65, 66, 70, 89, 93 and 94 are nitriles. PRM No. 34 is an ether. PRM No. 46 is an dioxane. PRM Nos. 47, 90 and 91 are dioxolanes.

In one aspect, the amount of total perfume based on total weight of starch encapsulates and starch agglomerates (Starch Encapsulated Accord (SEA)) ranges from 0.1% to about 99%, from 25% to about 95%, from 30 to about 90%, from 45% to about 90%, from 65% to about 90%. In one aspect, the PRMs disclosed in Table 1 and stereoisomers thereof are suitable for use in such starch encapsulates and starch agglomerates. Such PRMs and stereoisomers thereof may be used in combination in such starch encapsulates and starch agglomerates.

In another aspect, the amount of total perfume based on total weight of [cyclodextrin-perfume] complexes (Cyclodextrin (CD)) ranges from 0.1% to about 99%, from 2.5% to about 75%, from 5% to about 60%, from 5% to about 50%, from 5% to about 25%. In one aspect, the PRMs disclosed in Table 1 and stereoisomers thereof are suitable for use in such [cyclodextrin-perfume] complexes. Such PRMs and stereoisomers thereof may be used in combination in such [cyclodextrin-perfume] complexes.

In another aspect, the amount of total perfume based on total weight of Polymer Assisted Delivery (PAD) Matrix Systems (including Silicones) ranges from 0.1% to about 99%, from 2.5% to about 75%, from 5% to about 60%, from 5% to about 50%, from 5% to about 25%. In one aspect, the amount of total perfume based on total weight of a hot melt perfume delivery system/perfume loaded plastic Matrix System and ranges from 1% to about 99%, from 2.5% to about 75%, from 5% to about 60%, from 5% to about 50%, from 10% to about 50%. In one aspect, the PRMs disclosed in Table 1 and stereoisomers thereof are suitable for use in such Polymer Assisted Delivery (PAD) Matrix Systems, including hot melt perfume delivery system/perfume loaded plastic Matrix Systems. Such PRMs and stereoisomers thereof may be used in various combinations in such Polymer Assisted Delivery (PAD) Matrix Systems (including hot melt perfume delivery system/perfume loaded plastic Matrix Systems).

In one aspect, the amount of total perfume based on total weight of Amine Assisted Delivery (AAD) (including Aminosilicones) ranges from 1% to about 99%, from 2.5% to about 75%, from 5% to about 60%, from 5% to about 50%, from 5% to about 25%. In one aspect, the PRMs disclosed in Table 1 and stereoisomers thereof are suitable for use in such Amine Assisted Delivery (AAD) systems. Such PRMs and stereoisomers thereof may be used in various combinations in such Amine Assisted Delivery (AAD) systems. In one aspect, an Amine Assisted Delivery (AAD) system may comprise one or more PRMs selected from Table 1 Nos. 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39, 40, 41, 42, 43, 44, 45, 46, 47, 48, 49, 60, 62, 63, 64, 65, 66, 67, 68, 69, 70, 71, 72, 73, 74, 75, 76, 77, 78, 79, 80, 81, 82, 83, 84, 85, 86, 87, 88, 89, 90, 91, 92, 93, 94; stereoisomers of Table 1 Nos. 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39, 40, 41, 42, 43, 44, 45, 46, 47, 48, 49, 60, 62, 63, 64, 65, 66, 67, 68, 69, 70, 71, 72, 73, 74, 75, 76, 77, 78, 79, 80, 81, 82, 83, 84, 85, 86, 87, 88, 89, 90, 91, 92, 93, 94; and mixtures thereof.

PRM Nos. 4, 12, 13, 14, 23, 26, 27, 28, 29, 49, 52, 57, 58, 60, 67, 71, 73, 74 and 92 are ketones. PRM Nos. 6, 7, 17, 39, 40, 42, 45, 53, 64, 69, 84, 87 and 88 are aldehydes. PRM Nos. 5, 8, 9, 16, 21, 24, 30, 43, 51, 54, 59, 68, 72, 75, 76, 77, 78, 79, 80, 81, 82, 83, 85, and 86 are alcohols. PRM Nos. 25, 31, 32, 33, 37, 44 and 55 are esters. PRM Nos. 1, 2, 3, 10, 11, 15, 18, 19, 20, 22, 35, 36, 38, 41, 48, 50, 56, 61, 62, 63, 65, 66, 70, 89, 93 and 94 are nitriles. PRM No. 34 is an ether. PRM No. 46 is an dioxane. PRM Nos. 47, 90 and 91 are dioxolanes.

In one aspect, a Pro-Perfume (PP) Amine Reaction Product (ARP) system may comprise one or more PRMs selected from Table 1 Nos. 35, 36. Such PRMs are nitriles In one aspect, a Pro-Perfume (PP) Amine Reaction Product (ARP) system may comprise one or more PRMs selected from Table 1 Nos. 4, 12, 13, 14, 23, 26, 27, 28, 29, 49, 52, 57, 58, 60, 67, 71, 73, 74 and 92. Such PRMs are ketones. In one aspect, a Pro-Perfume (PP) Amine Reaction Product (ARP) system may comprise one or more PRMs selected from Table 1 Nos. 6, 7, 17, 39, 40, 42, 53, 64, 84, 87, 88. Such PRMs are aldehydes. In one aspect, the amount of total perfume based on total weight of Pro-Perfume (PP) Amine Reaction Product (ARP) system ranges from 0.1% to about 99%, from about 1% to about 99%, from 5% to about 90%, from 10% to about 75%, from 20% to about 75%, from 25% to about 60%.

The perfume delivery technologies (a.k.a., perfume delivery systems) that are disclosed in the present specification may be used in any combination in any type of consumer product, cleaning and/or treatment composition, fabric and hard surface cleaning and/or treatment composition, detergent, and/or highly compact detergent.

Perfumes

The PRMs disclosed in Table 1 may be used to formulate perfumes. Such perfumes are combinations of PRMs that may comprise a combination of Table 1 PRMs, or one or more Table 1 PRMs and one or more additional PRMs. When used in a perfume, the Table 1 PRMs may be employed, based on total perfume weight, at levels of from about 0.01% to about 50%, from about 0.1% to about 15%, from about 0.1% to about 10% or even from about 0.5% to about 10%. Such perfumes may be utilized in various applications, including being applied neat to a situs or used in a consumer product, cleaning and/or treatment composition, fabric and hard surface cleaning and/or treatment composition, detergent, and/or a highly compact detergent.

Adjunct Materials

For the purposes of the present invention, the non-limiting list of adjuncts illustrated hereinafter are suitable for use in the compositions detailed herein (e.g., consumer products, cleaning and/or treatment compositions, fabric and hard surface cleaning and/or treatment compositions, detergents, and/or a highly compact detergents). Such adjunct materials may be desirably incorporated in certain embodiments of the compositions, for example to assist or enhance performance of the composition, for treatment of the substrate to be cleaned, or to modify the aesthetics of the composition as is the case with perfumes, colorants, dyes or the like. It is understood that such adjuncts are in addition to the components that are supplied via Applicants' perfumes and/or perfume systems detailed herein. The precise nature of these additional components, and levels of incorporation thereof, will depend on the physical form of the composition and the nature of the operation for which it is to be used.

Suitable adjunct materials include, but are not limited to, surfactants, builders, chelating agents, dye transfer inhibiting agents, dispersants, enzymes, and enzyme stabilizers, catalytic materials, bleach activators, polymeric dispersing agents, clay soil removal/anti-redeposition agents, brighteners, suds suppressors, dyes, additional perfume and perfume delivery systems, structure elasticizing agents, fabric softeners, carriers, hydrotropes, processing aids and/or pigments. In addition to the disclosure below, suitable examples of such other adjuncts and levels of use are found in U.S. Pat. Nos. 5,576,282, 6,306,812 B1 and 6,326,348 B1.

Each adjunct ingredient is not essential to Applicants' compositions. Thus, certain embodiments of Applicants' compositions may not contain one or more of the following adjuncts materials: bleach activators, surfactants, builders, chelating agents, dye transfer inhibiting agents, dispersants, enzymes, and enzyme stabilizers, catalytic metal complexes, polymeric dispersing agents, clay and soil removal/anti-redeposition agents, brighteners, suds suppressors, dyes, additional perfumes and perfume delivery systems, structure elasticizing agents, fabric softeners, carriers, hydrotropes, processing aids and/or pigments. However, when one or more adjuncts are present, such adjuncts may be present as detailed below:

Surfactants—The compositions according to the present invention can comprise a surfactant or surfactant system wherein the surfactant can be selected from nonionic and/or anionic and/or cationic surfactants and/or ampholytic and/or zwitterionic and/or semi-polar nonionic surfactants. The surfactant is typically present at a level of from about 0.1%, from about 1%, or even from about 5% by weight of the cleaning compositions to about 99.9%, to about 80%, to about 35%, or even to about 30% by weight of the cleaning compositions.

Builders—The compositions of the present invention can comprise one or more detergent builders or builder systems. When present, the compositions will typically comprise at least about 1% builder, or from about 5% or 10% to about 80%, 50%, or even 30% by weight, of said builder. Builders include, but are not limited to, the alkali metal, ammonium and alkanolammonium salts of polyphosphates, alkali metal silicates, alkaline earth and alkali metal carbonates, aluminosilicate builders polycarboxylate compounds. ether hydroxypolycarboxylates, copolymers of maleic anhydride with ethylene or vinyl methyl ether, 1,3,5-trihydroxybenzene-2,4,6-trisulphonic acid, and carboxymethyl-oxysuccinic acid, the various alkali metal, ammonium and substituted ammonium salts of polyacetic acids such as ethylenediamine tetraacetic acid and nitrilotriacetic acid, as well as polycarboxylates such as mellitic acid, succinic acid, oxydisuccinic acid, polymaleic acid, benzene 1,3,5-tricarboxylic acid, carboxymethyloxysuccinic acid, and soluble salts thereof.

Chelating Agents—The compositions herein may also optionally contain one or more copper, iron and/or manganese chelating agents. If utilized, chelating agents will generally comprise from about 0.1% by weight of the compositions herein to about 15%, or even from about 3.0% to about 15% by weight of the compositions herein.

Dye Transfer Inhibiting Agents—The compositions of the present invention may also include one or more dye transfer inhibiting agents. Suitable polymeric dye transfer inhibiting agents include, but are not limited to, polyvinylpyrrolidone polymers, polyamine N-oxide polymers, copolymers of N-vinylpyrrolidone and N-vinylimidazole, polyvinyloxazolidones and polyvinylimidazoles or mixtures thereof. When present in the compositions herein, the dye transfer inhibiting agents are present at levels from about 0.0001%, from about 0.01%, from about 0.05% by weight of the cleaning compositions to about 10%, about 2%, or even about 1% by weight of the cleaning compositions.

Dispersants—The compositions of the present invention can also contain dispersants. Suitable water-soluble organic materials are the homo- or co-polymeric acids or their salts, in which the polycarboxylic acid may comprise at least two carboxyl radicals separated from each other by not more than two carbon atoms.

Enzymes—The compositions can comprise one or more detergent enzymes which provide cleaning performance and/or fabric care benefits. Examples of suitable enzymes include, but are not limited to, hemicellulases, peroxidases, proteases, cellulases, xylanases, lipases, phospholipases, esterases, cutinases, pectinases, keratanases, reductases, oxidases, phenoloxidases, lipoxygenases, ligninases, pullulanases, tannases, pentosanases, malanases, β-glucanases, arabinosidases, hyaluronidase, chondroitinase, laccase, and amylases, or mixtures thereof. A typical combination is a cocktail of conventional applicable enzymes like protease, lipase, cutinase and/or cellulase in conjunction with amylase.

Enzyme Stabilizers—Enzymes for use in compositions, for example, detergents can be stabilized by various techniques. The enzymes employed herein can be stabilized by the presence of water-soluble sources of calcium and/or magnesium ions in the finished compositions that provide such ions to the enzymes.

Catalytic Metal Complexes—Applicants' compositions may include catalytic metal complexes. One type of metal-containing bleach catalyst is a catalyst system comprising a transition metal cation of defined bleach catalytic activity, such as copper, iron, titanium, ruthenium, tungsten, molybdenum, or manganese cations, an auxiliary metal cation having little or no bleach catalytic activity, such as zinc or aluminum cations, and a sequestrate having defined stability constants for the catalytic and auxiliary metal cations, particularly ethylenediaminetetraacetic acid, ethylenediaminetetra (methyl-enephosphonic acid) and water-soluble salts thereof. Such catalysts are disclosed in U.S. Pat. No. 4,430,243.

If desired, the compositions herein can be catalyzed by means of a manganese compound. Such compounds and levels of use are well known in the art and include, for example, the manganese-based catalysts disclosed in U.S. Pat. No. 5,576,282. Cobalt bleach catalysts useful herein are known, and are described, for example, in U.S. Pat. Nos. 5,597,936 and 5,595,967. Such cobalt catalysts are readily prepared by known procedures, such as taught for example in U.S. Pat. Nos. 5,597,936, and 5,595,967.

Compositions herein may also suitably include a transition metal complex of a macropolycyclic rigid ligand—abbreviated as “MRL”. As a practical matter, and not by way of limitation, the compositions and cleaning processes herein can be adjusted to provide on the order of at least one part per hundred million of the benefit agent MRL species in the aqueous washing medium, and may provide from about 0.005 ppm to about 25 ppm, from about 0.05 ppm to about 10 ppm, or even from about 0.1 ppm to about 5 ppm, of the MRL in the wash liquor. Suitable transition-metals in the instant transition-metal bleach catalyst include manganese, iron and chromium. Suitable MRL's herein are a special type of ultra-rigid ligand that is cross-bridged such as 5,12-diethyl-1,5,8,12-tetraazabicyclo[6.6.2]hexa-decane. Suitable transition metal MRLs are readily prepared by known procedures, such as taught for example in WO 00/32601, and U.S. Pat. No. 6,225,464.

Methods of Use

Some of the consumer products disclosed herein can be used to clean or treat a situs inter alia a surface or fabric. Typically at least a portion of the situs is contacted with an embodiment of Applicants' composition, in neat form or diluted in a liquor, for example, a wash liquor and then the situs may be optionally washed and/or rinsed. In one aspect, a situs is optionally washed and/or rinsed, contacted with a particle according to the present invention or composition comprising said particle and then optionally washed and/or rinsed. For purposes of the present invention, washing includes but is not limited to, scrubbing, and mechanical agitation. The fabric may comprise most any fabric capable of being laundered or treated in normal consumer use conditions. Liquors that may comprise the disclosed compositions may have a pH of from about 3 to about 11.5. Such compositions are typically employed at concentrations of from about 500 ppm to about 15,000 ppm in solution. When the wash solvent is water, the water temperature typically ranges from about 5° C. to about 90° C. and, when the situs comprises a fabric, the water to fabric ratio is typically from about 1:1 to about 30:1.

Test Methods

It is understood that the test methods that are disclosed in the Test Methods Section of the present application should be used to determine the respective values of the parameters of Applicants' invention as such invention is described and claimed herein.

(1) C Log P

The “calculated log P” (C log P) is determined by the fragment approach of Hansch and Leo (cf., A. Leo, in Comprehensive Medicinal Chemistry, Vol. 4, C. Hansch, P. G. Sammens, J. B. Taylor, and C. A. Ramsden, Eds. P. 295, Pergamon Press, 1990, incorporated herein by reference). C log P values may be calculated by using the “C LOG P” program available from Daylight Chemical Information Systems Inc. of Irvine, Calif. U.S.A.

(2) Boiling Point

Boiling point is measured by ASTM method D2887-04a, “Standard Test Method for Boiling Range Distribution of Petroleum Fractions by Gas Chromatography,” ASTM International.

(3) Headspace Ratio

-   -   (a) Obtain a fragrance free consumer product formulation         (shampoo or leave-on conditioner).     -   (b) Obtain fragrance microcapsules whose water content has been         adjusted to achieve a perfume content of 25 wt % in the aqueous         slurry.     -   (c) Prepare Sample A by adding 2.0 grams of the fragrance         microcapsule aqueous slurry to 95 grams of the fragrance free         consumer product formulation. Then add 3.0 grams of deionized         water to balance the formulation to 100 grams. Age this         formulation for 1 week at 40 degrees Centigrade.     -   (d) Prepare Sample B by adding 0.50 grams of the neat fragrance         to 95 grams of fragrance free consumer product formulation. Then         add 4.5 grams of deionized water to balance the formulation to         100 grams. Age this formulation for 1 week at 40 degrees         Centigrade.

The Headspace Ratio for determining perfume leakage from a perfume delivery system is defined as the headspace concentration of Sample A divided by the headspace concentration of Sample B.

$\frac{H_{Sample\_ A}}{H_{Sample\_ B}},$ where H_(Sample) _(_) _(A) is the headspace concentration of a consumer product formulation Sample A, and H_(Sample) _(_) _(B) is the headspace concentration of a consumer product formulation Sample B.

The Headspace Ratio for determining perfume delivery efficiency from a perfume delivery system is defined as the headspace concentration of Sample B divided by the headspace concentration of Sample A,

$\frac{H_{Sample\_ B}}{H_{Sample\_ A}},$ where H_(Sample) _(_) _(A) is the headspace concentration of a consumer product formulation Sample A, and H_(Sample) _(_) _(B) is the headspace concentration of a consumer product formulation Sample B.

Solid-Phase Micro-Extraction (SPME)-Gas Chromatography/Mass Spectrometry is used to measure the level of perfume raw materials in the headspace of products. 1.0 grams of the 1 week at 40 degrees Centigrade aged sample (shampoo or conditioner) are placed into a clean 20 ml headspace vial and allowed to equilibrate for at least 2 hours at room temperature.

The samples are then analyzed using the MPS2-SMPE-GC-MS analysis system (GC-02001-0153, MSD-02001-0154, MPS2-02001-0155).

Apparatus:

-   1. 20 ml headspace vial -   2. Timer. -   3. Gas Chromatograph (GC): Agilent model 6890 with a CIS-4 injector     (Gerstel, Mulheim, Germany) and MPS-2 Autosampler and TDU. For SPME     analysis, we used the split/splitless injector (not the CIS-4     injector). -   4. GC column: J&W DB-5 MS, 30 M×0.25 mm ID, 1.0 m film thickness     obtained from J&W Scientific of Folsom, Calif., USA. -   5. Carrier gas, helium, 1.5 ml/min. flow rate. -   6. The injector liner is a special SPME liner (0.75 mm ID) from     Supelco. -   7. The Detector is a model 5973 Mass Selective Detector obtained     from Agilent Technologies, Inc., Wilmington, Del., USA having a     source temperature of about 230° C., and a MS Quad temperature of     about 150° C.     Analysis Procedure:     -   1. Transfer sample to proper sample tray and proceed with         SPME-GC-MS analysis.     -   2. Start sequence of sample loading and analysis. In this step,         the sample is allowed to equilibrate for at least two hours on         the auto sampler tray, then sampled directly from the tray. The         SPME fiber assembly is DVB/CAR/PDMS (50/30 um, 24 ga, 1 cm         length). Sampling time is 5 minutes.     -   3. Injector temperature is at 260 C.     -   4. Then GC-MS analysis run is started. Desportion time is 5         minutes.     -   5. The following temperature program is used:         -   i) an initial temperature of about 50° C. which is held for             3 minutes,         -   ii) increase the initial temperature at a rate of about 6°             C./min until a temperature of about 250° C. is reached, then             25° C./min to 275° C., hold at about 275° C. for 4.67             minute.     -   6. Perfume compounds are identified using the MS spectral         libraries of John Wiley & Sons and the National Institute of         Standards and Technology (NIST), purchased and licensed through         Hewlett Packard.     -   7. Chromatographic peaks for specific ions are integrated using         the Chemstation software obtained from Agilent Technologies,         Inc., Wilmington, Del., USA.     -   8. The ratio for each PRM is calculated by dividing the peak         area for the perfume raw material in Sample A by the peak area         in Sample B.     -   9. Each ratio is then weighted by that perfume raw material's         weight composition in the perfume.     -   10. The Headspace Ratio is calculated as the sum of the         individual perfume raw material ratios obtained in step 9.

(4) Perfume Leakage can Also be Evaluated Via % Liquid-Liquid Extraction and Gas Chromatographic-Mass Spectrometric Analysis

When determining the % perfume leakage from Perfume Microcapsules in liquid detergent, a fresh sample of liquid detergent with equal level of free perfume (without Perfume Microcapsules) must also be analyzed in parallel for reference.

1. Preparation of an Internal Standard Solution

-   -   Stock solution of tonalid: Weigh 70 mg tonalid and add 20 ml         hexane p.a.     -   Internal Standard Solution solution: Dilute 200 μl of stock         solution in 20 ml hexane p.a.     -   Mix to homogenize

2. Perfume Extraction from Liquid Detergent without Perfume Microcapsules (Reference)

-   -   Weigh 2 g of liquid detergent product into an extraction vessel     -   Add 2 ml of Internal Standard Solution and close vessel     -   Extract perfume by gently turning the extraction vessel         upside-down for 20 times (manually)     -   Add spoon tip of Sodium Sulphate     -   After separation of layers, immediately transfer hexane-layer         into Gas Chromatograph auto sampler-vial and cap vial     -   Inject splitless (1.5 μl) into Gas Chromatograph injection-port     -   Run Gas Chromatographic-Mass Spectrometric analysis

3. Perfume Extraction from Liquid Detergent with Perfume Microcapsules

-   -   Weigh 2 g of liquid detergent product into an extraction vessel     -   Add 2 ml of Internal Standard Solution and close vessel     -   Extract perfume by gently turning the extraction vessel         upside-down for 20 times (manually)     -   Add spoon tip of Sodium Sulphate     -   After separation of layers, immediately transfer hexane-layer         into Gas Chromatograph auto sampler-vial and cap vial     -   Inject splitless (1.5 μl) into Gas Chromatograph injection-port     -   Run Gas Chromatographic-Mass Spectrometric analysis

4. Calculation

-   -   The perfume leakage from capsules per individual Perfume Raw         Material:         % perfume leakage=((Area Perfume Raw Material caps×Area Internal         Standard Solution ref×Weight ref)/(Area Internal Standard         Solution caps×Area Perfume Raw Material ref×Weight caps))×100

(5) Odor Detection Threshold (ODT)

Determined using a gas chromatograph. The gas chromatograph is calibrated to determine the exact volume of material injected by the syringe, the precise split ratio, and the hydrocarbon response using a hydrocarbon standard of known concentration and chain length distribution. The air flow rate is accurately measured and, assuming the duration of human inhalation to last 12 seconds, the sampled volume is calculated. Since the precise concentration at the detector at any point in time is known, the mass per volume inhaled is known, and hence the concentration of material.

For example, to determine whether a material has a threshold below 50 parts per bullion, solutions are delivered to the sniff port at the calculated concentration. A panelist sniffs the GC effluent and identifies the retention time when odor is noticed. The average among 6 panelists determines the threshold of noticeability. The necessary amount of analyte is injected into the column to achieve a 50 parts per billion concentration at the detector. Typical gas chromatograph parameters for determining odor detection thresholds are listed below:

-   -   GC: 5890 Series II with FID detector, 7673 Autosampler     -   Column: J&W Scientific DB-1     -   Length: 30 meters, 0.25 millimeter inside diameter, 1 micrometer         film thickness     -   Method:         -   split injection: 17/1 split ratio         -   Autosampler: 1.13 microliters per injection         -   Column flow: 1.10 milliLiters per minute         -   Air Flow: 345 milliLiters per minute         -   Inlet Temperature: 245 degrees Centigrade         -   Detector Temperature: 285 degrees Centigrade         -   Initial Temperature=50 degrees Centigrade, 5 degrees             Centigrade per minute ramp rate, final temperature=280             degrees Centigrade, Final time=6 minutes         -   Leading assumptions: 12 seconds per sniff, GC air adds to             sample dilution

EXAMPLES

While particular embodiments of the present invention have been illustrated and described, it would be obvious to those skilled in the art that various other changes and modifications can be made without departing from the spirit and scope of the invention. It is therefore intended to cover in the appended claims all such changes and modifications that are within the scope of this invention.

Example 1: Synthesis of Table 1 Molecules

Synthesis of Table 1 Molecule Nos. 1, 3, 15, 18, 19, 20, 38, 41, 48, 50, 56, 62, 63, 65, 66, 93 & 94:

applied scale No. R¹ R² X (mmol substrate) 1 Me

Cl 66 3 2R¹ = cyclopropyl

Br 67 15 Me

Cl 11 18 H

Cl 12 19 Me, H

Cl 12 20 2R¹ = cyclobutyl

Cl 12 38 H

Br 33 41 Me, H

Br 22 48 Me

I 72 50 2R¹ = cyclobutyl

I 62 56 2R¹ = cyclopropyl

I 71 62 H

I 59 63 Me, H

I 48 65

Br 11 66

I 49 93

I 49 94

I 15 Used for synthesis of molecule 45 2R¹ = cyclopropyl

Br 54

A representative procedure is provided for the synthesis of Table 1 Molecule No. 50.

A solution of n-butyllithium (2.2M in cyclohexane—1 eq.) was added drop wise to an ice cold solution of diisopropylamine (1 eq.) in dry THF (0.5 M). After stirring for 10 minutes at this temperature, cyclobutanecarbonitrile (1 eq.) was added to the mixture. 5-Iodo-2-methylpent-2-ene (1 eq.) was added after another mixing of 10 minutes at 0° C. Reaction conversion was followed by GC-MS and seen as complete after 15 minutes stirring at 0° C. The reaction was quenched by addition of a saturated NH₄Cl aqueous solution and extracted with Et₂O. The combined organic layers were dried over MgSO₄ and concentrated under reduced pressure. The resulting oil was purified using a quick filtration over silica by elution with a petroleum ether-Et₂O mixture (9-1). Concentration of the eluent under reduced pressure resulted in the compound as a colorless oil (97% yield).

Synthesis of Table 1 Molecule Nos. 2, 10, 11, 22, 61:

applied scale (mmol No. R¹ R² X substrate)  2 Me

52 10 Me

Br 12 11 H

Br 6 22 Me

I 54 61 Me

I 27 Synthesis of Table 1 Molecule Nos. 4, 12, 13, 14, 23, 49, 52, 57, 58 & 67:

applied scale No. Nitrile R¹ R² R³ R⁴ (mmol substrate) 4 1 Me Me

Me 20 12 2 Me

s-Bu  8 13 3 R¹R² = cyclopropyl

Me 12 14 3 R¹R² = cyclopropyl

n-Bu 17 23 22 Me

n-Bu 22 49 48 Me Me

Me 23 52 50 R¹R² = cyclopropyl

Me 25 57 56 R¹R² = cyclopropyl

Me 24 58 56 R¹R² = cyclopropyl

n-Bu 10 67 66 Me

Me 21

A representative procedure is given for the synthesis of Table 1 Molecule No. 67.

A methyllithium solution (1.2 equiv.) was added drop wise to a solution of the nitrile (1 eq.) in dry THF (0.5M) at −20° C. After stirring for 15 minutes at −10/−20° C., full conversion was observed by GC-MS. The reaction was quenched with a H₂SO₄ solution (2M-2 eq.) and stirred at ambient temperature till full hydrolysis of the in situ formed imine was observed. The mixture was then extracted with Et₂O and washed with a saturated NaHCO₃ aqueous solution. The combined organic phases were dried over MgSO₄ and concentrated under reduced pressure. The resulting oil was purified using a quick filtration over silica gel by eluting with a petroleum ether—Et₂O mixture (9-1). Concentration of the eluent under reduced pressure resulted in the compound as a colorless oil (94% yield).

Synthesis of Table 1 Molecule Nos. 5, 8, 9, 16, 21, 24, 30, 51, 54, 59 & 68:

applied scale Carbonyl (mmol No. Compound R¹ R² R³ R⁴ substrate) 5 4 Me Me

Me 10 8 7 Me

H 11 9 6 Me Me

H 10 16 14 R¹R² = cyclopropyl

n-Bu 8 21 17 Me Me

H 8 24 23 Me

n-Bu 9 30 29 H H

Me 7 51 49 Me Me

Me 21 54 52 R¹R² = cyclobutyl

Me 12 59 57 R¹R² = cyclopropyl

Me 11 68 67 Me

Me 10

A representative procedure is given for the synthesis of Table 1 Molecule No. 68.

To a solution of compound 67 (1 eq.) in dry THF (0.5 M) was added portion wise lithium-aluminumhydride (0.5 eq.) at 0° C. Reaction completion was observed by GC-MS after 15 minutes of stirring at ambient temperature. The mixture was cooled to 0° C. and consequently was added: water (same amount of mL as mg hydride used), 15% NaOH solution (same amount of mL as mg hydride used) & water (2 times amount of mL as mg hydride used). This quenching was followed by stirring for 1 hour at ambient temperature. The resulting mixture was filtered over celite and the filter was washed with Et₂O. Concentration of the filtrate under reduced pressure resulted in the compound as a colorless oil (100% yield).

Synthesis of Table 1 Molecule Nos. 6, 7, 17, 39, 40, 42, 45, 53, 64 & 69:

applied scale No. Nitrile R¹ R² R³ (mmol substrate) 6 1 Me Me

22 7 2 Me

23 17 15 Me Me

18 39 18 H H

17 40 38 H H

19 42 41 Me H

9 45 Described in ketone synthesis R¹R² = cyclopropyl

51 53 50 R¹R² = cyclobutyl

12 64 61 Me

9 69 66 Me

12

A representative procedure is given for the synthesis of Table 1 Molecule No. 40.

To a solution of compound 38 (1 eq.) in dry CH₂Cl₂ (0.5 M) at −60° C. was added drop wise a diisobutylaluminiumhydride (1.3 eq.) solution (1.1 M cyclohexane). The resulting mixture was allowed to warm to ambient temperature for 2 hours. Reaction completion was observed by GC-MS. The mixture was cooled to 0° C. and a saturated aqueous sodium potassium tartrate solution was added carefully. This quenching was followed by stirring for 2 hours at ambient temperature. The resulting mixture was extracted with CH₂Cl₂, dried over MgSO₄ and reduced under reduced pressure to yield the pure aldehyde (99% yield).

Synthesis of carboxylic acids used for the synthesis of Table 1 Molecule Nos. 26, 27, 28, 29, 30, 31, 32, 33, 37 & 60:

applied scale No. R (mmol substrate) Used for synthesis molecules 26 & 27

57 Used for synthesis molecules 28, 29, 30 & 37

46 Used for synthesis molecules 31, 32, 33 & 60

209

To a solution of the phosphonium bromide [50889-29-7] (1.2 eq.) in dry THF (0.3 M) was added KHMDS (Potassiumhexamethyldisilazane—2.4 eq.) at ambient temperature. After stirring for 30 minutes at the same temperature, a solution of ketone/aldehyde (1 eq.) in dry THF (0.3 M) was added drop wise. The mixture was stirred for 3 hours, quenched with water (0.3 M) and extracted with Et₂O. The resulting water layer was acidified with a HCl aqueous solution (10%) till pH 2 was obtained. This mixture was extracted with Et₂O and the extracts were dried over MgSO₄ and concentrated under reduced pressure. The resulting oil was purified using a quick filtration over silica gel by eluting with a petroleum ether-Et₂O mixture (1-1). Concentration under reduced pressure resulted in the compound as a slightly yellow oil. (90-95% yield).

Synthesis of Table 1 Molecule Nos. 26, 27, 28, 29 & 60:

applied scale No. R¹ R² M (mmol substrate) 26

Me MgBr 11 27

Et MgBr 9 28

Et MgBr 11 29

Me MgBr 23 60

Me Li 25 Step 1.

To a solution of the acid formed in step 1 (1 eq.) in dry CH₂Cl₂ (0.5 M) was added 1,1′-carbonyldiimidazole (1 eq.) at ambient temperature. The mixture was stirred for 15 minutes and N,O-Dimethylhydroxylamine hydrochloride (1 eq.) was added. Stirring was continued at the same temperature for 1 hour and the mixture was quenched with an aqueous HCl solution (1 M-1.1 eq.). The aqueous layer was extracted with Et₂O, washed with NaHCO₃ and dried over MgSO₄. Concentration under reduced pressure resulted in the compound as a colorless oil. (86-95% yield)

Step 2.

The Weinreb amide formed in step 2 was solved in dry THF (0.5 M) and cooled to −15° C. A solution of cyclopropylmagnesium bromide (prepared from cyclopropyl bromide and magnesium turnings in THF—2 eq.) was added drop wise to the mixture. Complete reaction conversion was observed with GC-MS after 30 minutes stirring at 0° C. This reaction mixture was quenched with a saturated aqueous NH₄Cl solution, extracted with Et₂O; dried over MgSO₄ and concentrated under reduced pressure. The resulting oil was purified using a quick filtration over silica gel by eluting with a petroleum ether-Et₂O mixture (9-1). Concentration under reduced pressure resulted in the compound as a colorless oil. (62-75% yield)

Synthesis of Table 1 Molecule Nos. 31, 32, 33 & 37:

applied scale No. R¹ R² (mmol substrate) 31

n-Pr 13 32

Me 13 33

Et 13 37

Me 9

A representative procedure is given for the synthesis of Table 1 Molecule No. 37.

A solution of the carboxylic acid (1 eq.), methanol (2 eq.) and the Ishihara catalyst dimesitylammonium pentafluorobenzenesulfonate [850629-65-1] (1 mol %) in heptane (0.5 M) was heated at 60° C. Reaction completion was observed by GC-MS after 3 hours stirring. The mixture was then washed with an aqueous HCl solution (1 M). The organic phase was dried over MgSO₄ and concentrated under reduced pressure. The resulting oil was purified using a quick filtration over silica gel by eluting with a petroleum ether-Et₂O mixture (9-1). Concentration of the eluent under reduced pressure resulted in the compound as a colorless oil (93% yield).

Synthesis of Table 1 Molecule Nos. 34, 44 & 55:

applied scale No. Alcohol R R¹ X (mmol substrate) 34

Br 8 44 43

Me I 9 55 51

Me I 10

A representative procedure is given for the synthesis of Table 1 Molecule No. 55.

To a solution of alcohol 51 (1 eq.) in dry THF (0.5 M) was added sodium hydride (1.1 eq.) and iodomethane (1.5 eq.) at 0° C. The resulting mixture was allowed to stir at ambient temperature for 3 hours. The reaction was quenched with an aqueous saturated solution of ammonium chloride and subsequently extracted with Et₂O. The combined organic phases were dried over MgSO₄ and reduced under reduced pressure. The resulting oil was purified using a quick filtration over silica gel by eluting with a petroleum ether-Et₂O mixture (9-1). Concentration under reduced pressure resulted in the compound as a colorless oil (99% yield).

Synthesis of Table 1 Molecule No. 25:

To a solution of sodium hydride (1 eq.) and di-iso-propylamine (1 eq.) in dry THF (0.5 M), was added drop wise propionic acid (1 eq.) at 0° C. The resulting mixture was stirred for 10 minutes at ambient temperature and successively cooled to 0° C. again. Drop wise addition of n-butyllithium (1 eq., 2.2 M cyclohexene) was followed by stirring at reflux temperature for 5 minutes. The mixture was cooled to 0° C. and prenyl bromide was added. Stirring for 1 hour resulted in full conversion of the acid. The reaction was quenched with ice cold water (same amount as THF) and extracted with diethyl ether. The water layer was treated with an aqueous HCl solution (5 M) till pH 2 and again extracted with diethyl ether. The combined organic phases were dried over MgSO₄ and concentrated under reduced pressure to yield the pure acid (100% yield).

A solution of the carboxylic acid (1 eq.), i-butanol (2 eq.) and the Ishihara catalyst dimesitylammonium pentafluorobenzenesulfonate [850629-65-1] (1 mol %) in heptane (0.5 M) was heated at 60° C. Reaction completion was observed by GC-MS after 3 hours stirring.

The mixture was then washed with an aqueous HCl solution (1 M). The organic phase was dried over MgSO₄ and concentrated under reduced pressure. The resulting oil was purified using a quick filtration over silica gel by eluting with a petroleum ether-Et₂O mixture (9-1). Concentration of the eluent under reduced pressure resulted in the compound as a colorless oil (89% yield).

Synthesis of Table 1 Molecule Nos. 35 & 36:

A representative procedure is given for the synthesis of Table 1 Molecule No. 35.

An n-butyllithium solution (1.2 eq., 2.2 M cyclohexane) was added drop wide to a solution of acetonitrile (1.25 eq.) in dry THF at −60° C. After stirring for 15 minutes, (−)-myrtenal (1 eq.) was added to this mixture and subsequently stirred for 30 minutes at ambient temperature. Magnesium bromide (1.1 eq.) was added to this mixture followed by stirring for 15 minutes at the same temperature. Hereafter, a solution of methylmagnesium bromide was added and stirred finally for 1 hour at ambient temperature. The reaction was quenched with a saturated aqueous NH₄Cl solution and extracted with diethyl ether. The combined organic phases were dried over MgSO₄ and concentrated under reduced pressure. The resulting oil was purified using a quick filtration over silica gel by eluting with a petroleum ether-Et₂O mixture (9-1). Concentration of the eluent under reduced pressure resulted in the compound as a colorless oil (86% yield).

Synthesis of Table 1 Molecule No. 43:

To a solution of (−)-myrtenol (1 eq.) and di-iodomethane (3 eq.) in dry toluene, was added drop wise a solution of diethyl zinc (1 M) at −50° C. Full conversion was observed within 2 hours stirring at ambient temperature. The reaction was quenched at 0° C. by the addition of an aqueous HCl solution (1 M) and extracted with diethyl ether. The combined organic phases were dried over MgSO₄ and concentrated under reduced pressure. The resulting oil was purified using a quick filtration over silica gel by eluting with a petroleum ether-Et₂O mixture (9-1). Concentration of the eluent under reduced pressure resulted in the compound as an orange oil (99% yield).

Synthesis of Table 1 Molecule Nos. 46 & 47:

A representative procedure is given for the synthesis of Table 1 Molecule No. 47.

A mixture of the aldehyde 45 (1 eq.), ethanediol (1.2 eq.) and the catalyst Zirconium(IV) oxychloride octahydrate (5 mol %) in cyclohexane (0.5 M) was heated to reflux in a Dean-Stark apparatus for 5 hours to give full conversion. The reaction was quenched by the addition of an aqueous NH₄Cl solution and extracted with diethyl ether. The combined organic phases were dried over MgSO₄ and concentrated under reduced pressure. The resulting oil was purified using a quick filtration over silica gel by eluting with a petroleum ether-Et₂O mixture (9-1). Concentration of the eluent under reduced pressure resulted in the compound as an orange oil (89% yield).

Synthesis of Table 1 Molecule No. 70:

A solution of ethyl vanillin (1 eq., 18 mmol) and hydroxylamine hydrochloride (1.2 eq.) in acetonitrile (1 M) was stirred for 1 h 30 at reflux temperature. The reaction was quenched with water and extracted with diethyl ether. The organic layers were washed with a saturated aqueous NaHCO₃ solution, dried over MgSO₄ and concentrated under reduced pressure. Recrystallization from di-iso-propyl ether delivered the pure nitrile as white crystals (85% yield).

Synthesis of Table 1 Molecule No. 71:

A methyllithium solution (2.1 equiv., 6 mmol) was added drop wise to a solution of the nitrile 70 (1 eq.) in dry THF (0.5M) at −20° C. After stirring for 1 hour at ambient temperature, full conversion was observed by GC-MS. The reaction was quenched with a H₂SO₄ solution (2M-2 eq.) and stirred at ambient temperature till full hydrolysis of the in situ formed imine was observed (2 hours). The mixture was then extracted with Et₂O and washed with a saturated NaHCO₃ aqueous solution. The combined organic phases were dried over MgSO₄ and concentrated under reduced pressure. Recrystallization from di-iso-propyl ether delivered the pure ketone as white crystals (91% yield).

Synthesis of Table 1 Molecule No. 72:

A methylmagnesium bromide solution (2.5 equiv., 3 M) was added drop wise to a solution of ethyl vanillin (1 eq., 30 mmol) in dry THF (0.25M) at 0° C. After stirring for 1 hour at ambient temperature, full conversion was observed by GC-MS. The reaction was quenched with a NH₄Cl solution and extracted with Et₂O, dried over MgSO₄ and concentrated under reduced pressure. Recrystallization from di-iso-propyl ether delivered the pure ketone as white crystals (67% yield).

Synthesis of Table 1 Molecule Nos. 75, 76, 77, 78, 79, 80, 81, 82, 83, 85, 86, 90 & 91:

applied scale (mmol No. R R′ R″ R₁ R₂ R₃ R₄ R₅ R₆ substrate) 75 O O H — — Me H H H 12 76 O O H — — H H Me Me 12 77 O O H — — Me Me H H 12 78 O O H Et H — — — — 12 79 O O H Me H — — — — 12 80 O O H Me Me — — — — 12 81 O O H t-Bu H — — — — 12 82 O O H H H — — — — 12 83 O O H — — H H H H 12 85 O S H H H — — — — 12 86 O O H n-Bu H — — — — 12 90 O O Me Me H — — — — 12 91 O O Me Me Me — — — — 12

A representative procedure is given for the synthesis of Table 1 Molecule No. 77.

A mixture of the aldehyde (1 equiv.), the diol (or thio glycol—molecule 85) (2 equiv.) and the catalyst ZrOCl₂.8H₂O (0.05 equiv.) in toluene (0.5 M) was refluxed under Dean-Stark conditions till full conversion was observed by GC-MS analysis (1 to 2 h). The resulting reaction mixture was concentrated under reduced pressure and re-dissolved in Et₂O. This ether layer was washed with a saturated NaHCO₃ aqueous solution, dried over MgSO₄ and concentrated under reduced pressure. Toluene residues were removed under high vacuum which resulted in the pure compound (99% yield).

Synthesis of Table 1 Molecule No. 73:

To a mixture of delta-damascone (1 equiv. —104 mmol) and NaHCO₃ (1 equiv.) in CH₂Cl₂ (0.2M) was added meta-chloroperbenzoic acid (1.1 equiv.) at 0° C. The resulting reaction mixture was stirred at ambient temperature for 2 hours. Full conversion was observed by GC-MS analysis. The mixture was washed twice with water and filtered over a path of Celite®, which was rinsed with CH₂Cl₂. The organic phase was concentrated under reduced pressure to yield the epoxide 73 (99% yield).

Synthesis of Table 1 Molecule No. 74:

To a solution of the epoxide (1 equiv. —15 mmol) in MeOH (0.5 M) was added methane-sulfonic acid (0.01 equiv.) at ambient temperature. The resulting mixture was stirred at the same temperature for 9 hours. Full conversion was observed by GC-MS analysis. The mixture was quenched by the addition of 10 mL of a saturated NaHCO₃ aqueous solution and extracted with Et₂O. The organic layer was dried over MgSO₄ and concentrated under reduced pressure to yield the pure product (76% yield).

Synthesis of Table 1 Molecule No. 92:

Step 1. A mixture of the epoxide table 1 molecule number (1 equiv. —19 mmol), NaI (3 equiv.), CeCl₃.7H₂O (1.2 equiv.) in acetonitrile (0.5 M) was stirred at 40° C. for 2 hours. Full conversion was observed by GC-MS. The reaction was quenched by the addition of water and extracted with Et₂O. The organic phase was washed with an aqueous Na₂S₂O₃ solution, dried over MgSO₄ and concentrated under reduced pressure. This yielded the pure product (70% yield).

Step 2. A catalytic amount of DMAP (0.05 equiv.) was added to a mixture of the iodohydrine (1 equiv. —10 mmol), pyridine (1.5 equiv.) and acetic anhydride (2 equiv.) in CH₂Cl₂ (0.5 M) at ambient temperature. Full conversion was observed after 1 hour by GC-MS analysis. The reaction was quenched by the addition of water and extracted with Et₂O. The organic phase was washed with an aqueous 1M HCl solution, dried over MgSO₄ and concentrated under reduced pressure. This yielded the pure product (95% yield).

Step 3. A solution of the iodide (1 equiv. —15 mmol) and DBU (2 equiv.) in toluene (0.5 M) was stirred for 2 hours at 70° C. Full conversion was observed by GC-MS analysis. The reaction was concentrated under reduced pressure and retaken in Et₂O, washed with an aqueous 1M HCl solution, dried over MgSO₄ and again concentrated under reduced pressure. This resulted in pure allylic acetate (96% yield).

Step 4. An aqueous solution of NaOH (0.3 M-2N solution) was added to a solution of the acetate (1 equiv.) in THF (0.5 M) at ambient temperature. This mixture was heated to 60° C. and stirred over night to yield full conversion (GC-MS). The reaction mixture was extracted with Et₂O, washed with water, dried over MgSO₄ and concentrated under reduced pressure. Purification by column chromatography (eluens: petroleum ether/Et₂O—1/1) yielded the pure product (62% yield).

Synthesis of Table 1 Molecule Nos. 84 & 87:

applied scale No. R (mmol substrate) 84 n-Bu 15 87 n-pentyl 15

A representative procedure is given for the synthesis of Table 1 Molecule No. 84.

A mixture of n-BuOH (1.3 M-12 mL) and sodium metal (4 eq.) was heated at 110° C. till all sodium was dissolved. DMF (1.3 M-12 mL) was added to this mixture at ambient temperature and degassed under reduced pressure. CuCl (1.45 equiv.) was added and stirred for 10 minutes at the same temperature. After adding the bromide (1 equiv.), the mixture was heated to 120° C. Full conversion was observed after 30 minutes by GC-MS analysis. The resulting reaction mixture was acidified with an aqueous solution of HCl (2 M), extracted with EtOAc, washed with water and dried over MgSO₄. Concentration under reduced pressure resulted in a brown oil which was purified by column chromatography (eluens: petroleum ether/EtOAc—8/2). The product was isolated as a yellow oil (77% yield).

Synthesis of Table 1 Molecule No. 88:

To a suspension of ethyl vanillin (1 equiv. —120 mmol) and iodomethane (1.5 equiv.) in an aqueous NaOH solution (1 M-5 N solution) was added phase transfer catalyst Aliquat 336 (0.1 equiv.). The mixture was refluxed for 1 hour which resulted in full conversion, observed by GC-MS analysis. By cooling the mixture to 0° C. under continuously stirring, a white precipitate formed. Filtration of the precipitate and recrystallization from i-Pr₂O yielded the product as white crystals (74% yield).

Synthesis of Table 1 Molecule No. 89:

A mixture of the aldehyde table 1 molecule number 88 (1 equiv. —22 mmol) and hydroxylamine hydrochloride (1.4 equiv.) in acetonitrile (1 M) was refluxed for 2 hours, which resulted in full conversion observed by GC-MS analysis. The reaction was quenched by the addition of water (40 mL) and extracted with Et₂O. Concentration of the organic phase under reduced pressure was followed by a recrystallization from i-Pr₂O. This resulted in the pure nitrile (54% yield).

Example 2: Preformed Amine Reaction Product

The following ingredients are weighted off in a glass vial:

-   -   1. 50% of the perfume material comprising one or more Table 1         PRMs     -   2. 50% of Lupasol WF (CAS#09002-98-6) from BASF, is put at         60° C. in warm water bath for 1 hour before use.

Mixing of the two ingredients is done by using the Ultra-Turrax T25 Basic equipment (from IKA) during 5 minutes. When the mixing is finished the sample is put in a warm water bath at 60° C. for ±12 hours. A homogenous, viscous material is obtained.

In the same way as described above different ratios between the components can be used:

Weight % Perfume Material 40 50 60 70 80 Lupasol WF 60 50 40 30 20

Example 3: 84 Wt % Core/16 wt % Wall Melamine Formaldehyde (MF) Capsule (PAD Reservoir System

25 grams of butyl acrylate-acrylic acid copolymer emulsifier (Colloid C351, 25% solids, pka 4.5-4.7, (Kemira Chemicals, Inc. Kennesaw, Ga. U.S.A.) is dissolved and mixed in 200 grams deionized water. The pH of the solution is adjusted to pH of 4.0 with sodium hydroxide solution. 8 grams of partially methylated methylol melamine resin (Cymel 385, 80% solids, (Cytec Industries West Paterson, N.J., U.S.A.)) is added to the emulsifier solution. 200 grams of perfume oil comprising one or more Table 1 PRMs is added to the previous mixture under mechanical agitation and the temperature is raised to 50° C. After mixing at higher speed until a stable emulsion is obtained, the second solution and 4 grams of sodium sulfate salt are added to the emulsion. This second solution contains 10 grams of butyl acrylate-acrylic acid copolymer emulsifier (Colloid C351, 25% solids, pka 4.5-4.7, Kemira), 120 grams of distilled water, sodium hydroxide solution to adjust pH to 4.8, 25 grams of partially methylated methylol melamine resin (Cymel 385, 80% solids, Cytec). This mixture is heated to 70° C. and maintained overnight with continuous stirring to complete the encapsulation process. 23 grams of acetoacetamide (Sigma-Aldrich, Saint Louis, Mo., U.S.A.) is added to the suspension. An average capsule size of 30 um is obtained as analyzed by a Model 780 Accusizer.

Example 4: Process of Making a Polymer Assisted Delivery (PAD) Matrix System

A mixture comprising 50% of a perfume composition comprising one or more Table 1 PRMs, 40% of carboxyl-terminated Hycar®1300X18 (CAS#0068891-50-9) from Noveon, (put at 60° C. in warm water bath for 1 hour before mixing) and 10% of Lupasol® WF(CAS#09002-98-6) from BASF (put at 60° C. in warm water bath for 1 hour before mixing). Mixing is achieved by mixing for five minutes using a Ultra-Turrax T25 Basic equipment (from IKA). After mixing, the mixture is put in a warm water bath at 60° C. for ±12 hours. A homogenous, viscous and sticky material is obtained.

In the same way as described above different ratios between the components can be used:

Weight % Perfume composition 40 50 60 70 80 Lupasol ® WF 12 10 8 6 4 Hycar ® 48 40 32 24 16 CTBN1300X18

Weight % Perfume composition 50 50 50 50 50 50 50 50 Lupasol ® WF 2.5 5 7.5 10 12.5 15 17.5 20 Hycar ® CTBN 47.5 45 42.5 40 37.5 35 32.5 30 1300X18

Example 5: Product Formulation

Non-limiting examples of product formulations containing PRMs disclosed in the present specification perfume and amines summarized in the following table.

EXAMPLES (% wt) XI XII XIII XIV XV XVI XVII XVIII XIX XX FSA^(a) 14 16.47 14 12 12 16.47 — — 5 5 FSA^(b) — 3.00 — — — FSA^(c) — — 6.5  — — Ethanol 2.18 2.57 2.18 1.95 1.95 2.57 — — 0.81 0.81 Isopropyl — — — — — — 0.33 1.22 — — Alcohol Starch^(d) 1.25 1.47 2.00 1.25 — 2.30 0.5 0.70 0.71 0.42 Amine* 0.6 0.75 0.6 0.75 0.37 0.60 0.37 0.6  0.37 0.37 Perfume X^(e) 0.40 0.13 0.065 0.25 0.03 0.030 0.030  0.065 0.03 0.03 Phase 0.21 0.25 0.21 0.21 0.14 — — 0.14 — — Stabilizing Polymer^(f) Suds — — — — — — — 0.1  — — Suppressor^(g) Calcium 0.15 0.176 0.15 0.15 0.30 0.176 — 0.1-0.15 — — Chloride DTPA^(h) 0.017 0.017 0.017 0.017 0.007 0.007 0.20 — 0.002 0.002 Preservative 5 5 5 5 5 5 — 250^(j)    5 5 (ppm)^(i,j) Antifoam^(k) 0.015 0.018 0.015 0.015 0.015 0.015 — — 0.015 0.015 Dye 40 40 40 40 40 40 11 30-300 30 30 (ppm) Ammonium 0.100 0.118 0.100 0.100 0.115 0.115 — — — — Chloride HCl 0.012 0.014 0.012 0.012 0.028 0.028 0.016  0.025 0.011 0.011 Structurant^(l) 0.01 0.01 0.01 0.01 0.01 0.01 0.01 0.01 0.01 0.01 Additional 0.8 0.7 0.9 0.5 1.2 0.5 1.1 0.6  1.0 0.9 Neat Perfume Deionized † † † † † † † † † † Water ^(a)N,N-di(tallowoyloxyethyl)-N,N-dimethylammonium chloride. ^(b)Methyl bis(tallow amidoethyl)2-hydroxyethyl ammonium methyl sulfate. ^(c)Reaction product of Fatty acid with Methyldiethanolamine in a molar ratio 1.5:1, quaternized with Methylchloride, resulting in a 1:1 molar mixture of N,N-bis(stearoyl-oxy-ethyl) N,N-dimethyl ammonium chloride and N-(stearoyl-oxy-ethyl) N,-hydroxyethyl N,N dimethyl ammonium chloride. ^(d)Cationic high amylose maize starch available from National Starch under the trade name CATO ®. ^(e)Perfume comprising one or more Table 1 PRMs. ^(f)Copolymer of ethylene oxide and terephthalate having the formula described in U.S. Pat. No. 5,574,179 at co1.15, lines 1-5, wherein each X is methyl, each n is 40, u is 4, each R1 is essentially 1,4-phenylene moieties, each R2 is essentially ethylene, 1,2-propylene moieties, or mixtures thereof. ^(g)SE39 from Wacker ^(h)Diethylenetriaminepentaacetic acid. ^(i)KATHON ® CG available from Rohm and Haas Co. “PPM” is “parts per million.” ^(j)Gluteraldehyde ^(k)Silicone antifoam agent available from Dow Corning Corp. under the trade name DC2310. ^(l)Hydrophobically-modified ethoxylated urethane available from Rohm and Haas under the tradename Aculan 44. *One or more materials comprising an amine moiety as disclosed in the present specification. † balance

Example 6: Dry Laundry Formulations

% w/w granular laundry detergent composition Component A B C D E F G Brightener 0.1 0.1 0.1 0.2 0.1 0.2 0.1 Soap 0.6 0.6 0.6 0.6 0.6 0.6 0.6 Ethylenediamine disuccinic acid 0.1 0.1 0.1 0.1 0.1 0.1 0.1 Acrylate/maleate copolymer 1.5 1.5 1.5 1.5 1.5 1.5 1.5 Hydroxyethane di(methylene 0.4 0.4 0.4 0.4 0.4 0.4 0.4 phosphonic acid) Mono-C₁₂₋₁₄ alkyl, di-methyl, 0.5 0.5 0.5 0.5 0.5 0.5 0.5 mono-hydroyethyl quaternary ammonium chloride Linear alkyl benzene 0.1 0.1 0.2 0.1 0.1 0.2 0.1 Linear alkyl benzene sulphonate 10.3 10.1 19.9 14.7 10.3 17 10.5 Magnesium sulphate 0.4 0.4 0.4 0.4 0.4 0.4 0.4 Sodium carbonate 19.5 19.2 10.1 18.5 29.9 10.1 16.8 Sodium sulphate 29.6 29.8 38.8 15.1 24.4 19.7 19.1 Sodium Chloride 0.1 0.1 0.1 0.1 0.1 0.1 0.1 Zeolite 9.6 9.4 8.1 18 10 13.2 17.3 Photobleach particle 0.1 0.1 0.2 0.1 0.2 0.1 0.2 Blue and red carbonate speckles 1.8 1.8 1.8 1.8 1.8 1.8 1.8 Ethoxylated Alcohol AE7 1 1 1 1 1 1 1 Tetraacetyl ethylene diamine 0.9 0.9 0.9 0.9 0.9 0.9 0.9 agglomerate (92 wt % active) Citric acid 1.4 1.4 1.4 1.4 1.4 1.4 1.4 PDMS/clay agglomerates (9.5% wt 10.5 10.3 5 15 5.1 7.3 10.2 % active PDMS) Polyethylene oxide 0.2 0.2 0.2 0.2 0.2 0.2 0.2 Enzymes e.g. Protease (84 mg/g 0.2 0.3 0.2 0.1 0.2 0.1 0.2 active), Amylase (22 mg/g active) Suds suppressor agglomerate 0.2 0.2 0.2 0.2 0.2 0.2 0.2 (12.4 wt % active) Sodium percarbonate (having 7.2 7.1 4.9 5.4 6.9 19.3 13.1 from 12% to 15% active AvOx) Additional Neat Perfume** 0.5 0.5 0.5 0.5 0.5 0.5 0.5 Amine* 0.1 0.5 0.0 0.01 0.02 0.00 0.07 Perfume Delivery System As 0.05 0.0 0.1 0.0 0.2 0.4 0.0 Disclosed In The Present Specification Including Examples 2-4 Perfume comprising one or more 0.3 0.4 0.01 0.02 0.04 0.1 0.1 PRMs from Table 1 Water 1.4 1.4 1.4 1.4 1.4 1.4 1.4 Misc 0.1 0.1 0.1 0.1 0.1 0.1 0.1 Total Parts 100 100 100 100 100 100 100 *One or more materials comprising an amine moiety as disclosed in the present specification. **Optional

Example 7: Liquid Laundry Formulations (HDLs)

Ingredient HDL 1 HDL 2 HDL3 HDL4 HDL 5 HDL 6 Alkyl Ether Sulphate 0.00 0.50 12.0 12.0 6.0 7.0 Dodecyl Benzene 8.0 8.0 1.0 1.0 2.0 3.0 Sulphonic Acid Ethoxylated Alcohol 8.0 6.0 5.0 7.0 5.0 3.0 Citric Acid 5.0 3.0 3.0 5.0 2.0 3.0 Fatty Acid 3.0 5.0 5.0 3.0 6.0 5.0 Ethoxysulfated 1.9 1.2 1.5 2.0 1.0 1.0 hexamethylene diamine quaternized Diethylene triamine penta 0.3 0.2 0.2 0.3 0.1 0.2 methylene phosphonic acid Enzymes 1.20 0.80 0 1.2 0 0.8 Brightener (disulphonated 0.14 0.09 0 0.14 0.01 0.09 diamino stilbene based FWA) Cationic hydroxyethyl 0 0 0.10 0 0.200 0.30 cellulose Poly(acrylamide-co- 0 0 0 0.50 0.10 0 diallyldimethylammonium chloride) Hydrogenated Castor Oil 0.50 0.44 0.2 0.2 0.3 0.3 Structurant Boric acid 2.4 1.5 1.0 2.4 1.0 1.5 Ethanol 0.50 1.0 2.0 2.0 1.0 1.0 1,2 propanediol 2.0 3.0 1.0 1.0 0.01 0.01 Glutaraldehyde 0 0 19 ppm 0 13 ppm 0 Diethyleneglycol (DEG) 1.6 0 0 0 0 0 2,3-Methyl-1,3- 1.0 1.0 0 0 0 0 propanediol (M pdiol) Mono Ethanol Amine 1.0 0.5 0 0 0 0 NaOH Sufficient To pH 8 pH 8 pH 8 pH 8 pH 8 pH 8 Provide Formulation pH of: Sodium Cumene 2.00 0 0 0 0 0 Sulphonate (NaCS) Silicone (PDMS) emulsion 0.003 0.003 0.003 0.003 0.003 0.003 Additional Neat Perfume** 0.7 0.5 0.8 0.8 0.6 0.6 Amine* 0.01 0.10 0.0 0.10 0.20 0.05 Perfume comprising one or 0.02 0.15 0.0 0.2 0.3 0.1 more PRMs from Table 1 Perfume Delivery System 0.2 0.02 0.4 0.0 0.0 0.0 As Disclosed In The Present Specification Including Examples 2-4 Water Balance Balance Balance Balance Balance Balance *One or more materials comprising an amine moiety as disclosed in the present specification. **Optional.

Example 8: Shampoo Formulations

Ingredient Ammonium Laureth Sulfate (AE₃S)  6.00    Ammonium Lauryl Sulfate (ALS) 10.00    Laureth-4 Alcohol  0.90    Trihydroxystearin⁽⁷⁾  0.10    Perfume comprising one or more  0.60    PRMs from Table 1 Sodium Chloride  0.40    Citric Acid  0.04    Sodium Citrate  0.40    Sodium Benzoate  0.25    Ethylene Diamine Tetra Acetic Acid  0.10    Dimethicone^((9, 10, 11))  1.00⁽⁹⁾ Water and Minors (QS to 100%) Balance

Example 9: Fine Fragrance Formulations

Ingredient 1 2 3 Cyclic oligosaccharide 0 5 10 Ethanol 90 75 80 Perfume comprising one or more 10 20 10 PRMs from Table 1

The dimensions and values disclosed herein are not to be understood as being strictly limited to the exact numerical values recited. Instead, unless otherwise specified, each such dimension is intended to mean both the recited value and a functionally equivalent range surrounding that value. For example, a dimension disclosed as “40 mm” is intended to mean “about 40 mm”.

All documents cited in the Detailed Description of the Invention are, in relevant part, incorporated herein by reference; the citation of any document is not to be construed as an admission that it is prior art with respect to the present invention. To the extent that any meaning or definition of a term in this document conflicts with any meaning or definition of the same term in a document incorporated by reference, the meaning or definition assigned to that term in this document shall govern.

While particular embodiments of the present invention have been illustrated and described, it would be obvious to those skilled in the art that various other changes and modifications can be made without departing from the spirit and scope of the invention. It is therefore intended to cover in the appended claims all such changes and modifications that are within the scope of this invention. 

What is claimed is:
 1. A perfume raw material selected from the group consisting of 3-((1R,5S)-6,6-dimethylbicyclo[3.1.1]hept-2-en-2-yl)propanenitrile; (2R,S)-3-((1R,5S)-6,6-dimethylbicyclo[3.1.1]hept-2-en-2-yl)-2-methylpropanenitrile; and 1-(((1R,5S)-6,6-dimethyl-bicyclo[3.1.1]hept-2-en-2-yl)-methyl)cyclobutanecarbonitrile and stereoisomers of said perfume raw materials.
 2. A perfume raw material according to claim 1, said perfume raw material being 3-((1R,5S)-6,6-dimethylbicyclo[3.1.1]hept-2-en-2-yl)propanenitrile, or a stereoisomer of said perfume raw material.
 3. A perfume comprising a perfume raw material selected from the group consisting of 3-((1R,5S)-6,6-dimethylbicyclo[3.1.1]hept-2-en-2-yl)propanenitrile; (2R,S)-3-((1R,5S)-6,6-dimethylbicyclo[3.1.1]hept-2-en-2-yl)-2-methylpropanenitrile; 1-(((1R,5S)-6,6-dimethyl-bicyclo[3.1.1]hept-2-en-2-yl)-methyl)cyclobutanecarbonitrile, stereoisomers of said perfume raw materials; and mixtures thereof; and an additional perfume raw material.
 4. The perfume according to claim 3, said perfume comprising 3-((1R,5S)-6,6-dimethylbicyclo[3.1.1]hept-2-en-2-yl)propanenitrile, or a stereoisomer of said perfume raw material.
 5. A consumer product comprising, based on total consumer product weight, from about 0.0001% to about 25% of one or more perfume raw materials selected from the group consisting of 3-((1R,5S)-6,6-dimethylbicyclo[3.1.1]hept-2-en-2-yl)propanenitrile; (2R,S)-3-((1R,5S)-6,6-dimethylbicyclo[3.1.1]hept-2-en-2-yl)-2-methylpropanenitrile; 1-(((1R,5S)-6,6-dimethyl-bicyclo[3.1.1]hept-2-en-2-yl)-methyl)cyclobutanecarbonitrile; (E,Z)-3-((1R,5S)-6,6-dimethylbicyclo[3.1.1]hept-2-en-2-yl)acrylonitrile; 4-((1R,5S)-6,6-dimethylbicyclo[3.1.1]hept-2-en-2-yl)butanenitrile; stereoisomers of said perfume raw materials; and mixtures thereof; and an adjunct ingredient.
 6. A consumer product according to claim 5, said consumer product being a cleaning and/or treatment composition, said consumer product comprising an adjunct ingredient selected from the group consisting of surfactants, builders, enzymes, and enzyme stabilizers, clay soil removal/anti-redeposition agents, brighteners, suds suppressors, dyes, fabric softeners and mixtures thereof.
 7. A consumer product according to claim 5, said consumer product being a fabric and/or hard surface cleaning and/or treatment composition said consumer product comprising an adjunct ingredient selected from the group consisting of surfactants, builders, brighteners, suds suppressors, fabric softeners and mixtures thereof.
 8. A consumer product according to claim 5, said consumer product being a detergent, said detergent comprising, based on total detergent weight, from about 0.00001% to about 25% of one or more perfume raw materials selected from 3-((1R,5S)-6,6-dimethylbicyclo[3.1.1]hept-2-en-2-yl)propanenitrile; 4-((1R,5S)-6,6-dimethylbicyclo[3.1.1]hept-2-en-2-yl)butanenitrile; stereoisomers of said perfume raw materials; and mixtures thereof.
 9. A consumer product according to claim 5, said consumer product being a highly compacted consumer product, said highly compacted consumer product comprising, based on total highly compacted consumer product weight, from about 0.00001% to about 25% of one or more perfume raw material selected from 3-((1R,5S)-6,6-dimethylbicyclo[3.1.1]hept-2-en-2-yl)propanenitrile; 4-((1R,5S)-6,6-dimethylbicyclo[3.1.1]hept-2-en-2-yl)butanenitrile; stereoisomers of said perfume raw materials; and mixtures thereof.
 10. A consumer product according to claim 9, said consumer product being a highly compacted detergent, said highly compacted detergent comprising one or more perfume raw material selected from 3-((1R,5S)-6,6-dimethylbicyclo[3.1.1]hept-2-en-2-yl)propanenitrile; 4-((1R,5S)-6,6-dimethylbicyclo[3.1.1]hept-2-en-2-yl)butanenitrile; stereoisomers of said perfume raw materials; and mixtures thereof.
 11. A perfume delivery system comprising from 0.001% to about 50% of one or more perfume raw material selected from 3-((1R,5S)-6,6-dimethylbicyclo[3.1.1]hept-2-en-2-yl)propanenitrile; (2R,S)-3-((1R,5S)-6,6-dimethylbicyclo[3.1.1]hept-2-en-2-yl)-2-methylpropanenitrile; 1-(((1R,5S)-6,6-dimethyl-bicyclo[3.1.1]hept-2-en-2-yl)-methyl)cyclobutanecarbonitrile; (E,Z)-3-((1R,5S)-6,6-dimethylbicyclo[3.1.1]hept-2-en-2-yl)acrylonitrile; 4-((1R,5S)-6,6-dimethylbicyclo[3.1.1]hept-2-en-2-yl)butanenitrile; stereoisomers of said perfume raw materials; and mixtures thereof; wherein said perfume delivery system is selected from a polymer assisted delivery system; a molecule-assisted delivery system; a fiber-assisted delivery system; an amine assisted delivery system; a cyclodextrin delivery system; a starch encapsulated accord; an inorganic carrier delivery system; or a pro-perfume.
 12. The perfume delivery system of claim 11, said perfume delivery system comprising, one or more perfume raw material selected from 3-((1R,5S)-6,6-dimethylbicyclo[3.1.1]hept-2-en-2-yl)propanenitrile; 4-((1R,5S)-6,6-dimethylbicyclo[3.1.1]hept-2-en-2-yl)butanenitrile; stereoisomers of said perfume raw materials; and mixtures thereof.
 13. A perfume delivery system according to claim 12, said perfume delivery system being a starch encapsulated accord.
 14. A perfume delivery system, said perfume delivery system being selected from a nanocapsule or a microcapsule, a pro-perfume amine reaction product, an amine assisted delivery system, a polymer assisted delivery matrix system, and a cyclodextrin delivery system; said perfume delivery system comprising, based on total delivery system weight, from about 0.1% to about 99% of one or more perfume raw material selected from 3-((1R,5S)-6,6-dimethylbicyclo[3.1.1]hept-2-en-2-yl)propanenitrile; (2R,S)-3-((1R,5S)-6,6-dimethylbicyclo[3.1.1]hept-2-en-2-yl)-2-methylpropanenitrile; 1-(((1R,5S)-6,6-dimethyl-bicyclo[3.1.1]hept-2-en-2-yl)-methyl)cyclobutanecarbonitrile; (E,Z)-3-((1R,5S)-6,6-dimethylbicyclo[3.1.1]hept-2-en-2-yl)acrylonitrile; 4-((1R,5S)-6,6-dimethylbicyclo[3.1.1]hept-2-en-2-yl)butanenitrile; stereoisomers of said perfume raw materials; and mixtures thereof.
 15. A perfume delivery system, according to claim 14, comprising one or more perfume raw material selected from 3-((1R,5S)-6,6-dimethylbicyclo[3.1.1]hept-2-en-2-yl)propanenitrile; 4-((1R,5S)-6,6-dimethylbicyclo[3.1.1]hept-2-en-2-yl)butanenitrile; stereoisomers of said perfume raw materials; and mixtures thereof.
 16. A consumer product comprising, based on total consumer product weight, from about 0.001% to about 20% of a perfume delivery system comprising a perfume raw material selected from the group consisting of from 3-((1R,5S)-6,6-dimethylbicyclo[3.1.1]hept-2-en-2-yl)propanenitrile; 4-((1R,5S)-6,6-dimethylbicyclo[3.1.1]hept-2-en-2-yl)butanenitrile; stereoisomers of said perfume raw materials; and mixtures thereof. 